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Kingphar Medical Group

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10/6 2026

Table of Contents

Hygiene & Nursing · Product Specification

Disposable Underpads:
Specifications, Absorbency Levels
& Procurement Guide 2026

Complete technical breakdown of underpad construction, SAP core absorbency tiers, standard sizes, and OEM specification parameters — built for hospital procurement managers and B2B medical supply distributors.

5-Layer Construction SAP + Fluff Pulp Core Light / Moderate / Heavy Absorbency CE · ISO 13485 · FDA OEM Custom Sizes
A
Albar
Content Auditor & Content Operations · Kingphar Medical
Construction
5-Layer
NW + Tissue + Core + Tissue + PE
Absorbency Range
300–1,500 mL
Light to Super Absorbency
Standard Sizes
6 Sizes
17×24" to 36×36"
Certifications
CE · FDA
ISO 13485 QMS
Section 01

What Is a Disposable Underpad and Why Does Construction Matter?

A disposable underpad — also known commercially as a "chux pad," incontinence pad, or bed protector — is a multi-layer absorbent sheet designed to protect mattresses, chairs, wheelchairs, and operating surfaces from fluid contamination. Underpads are a staple procurement item in hospitals, nursing homes, post-acute care facilities, and home healthcare settings.

For procurement managers, the critical distinction is that not all underpads are equivalent. A low-cost underpad with a fluff-only core may hold 300 mL before strike-through, while a properly engineered SAP-enhanced pad of the same dimensions absorbs over 1,200 mL with a dry surface feel. The specification differences are entirely in the construction — and construction is what separates a reliable product from one that requires constant replacement, increases nursing workload, and contributes to moisture-associated skin damage (MASD).

Understanding the layered construction, absorbency grading, and size standardization allows procurement teams to write precise tender specifications that match clinical needs to cost-per-use rather than cost-per-unit.

Section 02

5-Layer Construction: Anatomy of a Disposable Underpad

Medical-grade disposable underpads follow a consistent 5-layer architecture. Each layer serves a specific function in the fluid management chain — from initial acquisition through distribution, absorption, retention, and barrier protection.

Layer 1: Nonwoven Topsheet (Skin Contact Surface)

The topsheet is the patient-facing surface, typically manufactured from hydrophilic spunbond polypropylene (SBPP) at 15–45 GSM. Its function is rapid fluid acquisition: drawing liquid away from the skin surface and transferring it downward into the absorbent core. Higher GSM topsheets (30–45 GSM) provide improved softness and reduced SAP particle migration, which is clinically important for pressure-injury-prone patients who remain on the pad for extended periods.

Layer 2: Tissue Acquisition-Distribution Layer

A tissue paper layer (typically 14–18 GSM) sits between the topsheet and the absorbent core. This layer serves two functions: it spreads incoming fluid laterally across a wider area of the core (improving utilization efficiency) and prevents direct contact between the wet core and the topsheet, maintaining the dry-surface effect.

Layer 3: Absorbent Core (Fluff Pulp + SAP)

The core is the performance-defining component. It consists of virgin cellulose fluff pulp blended with superabsorbent polymer (SAP) granules. The ratio of SAP to fluff pulp determines the absorbency tier:

Absorbency TierCore CompositionTypical CapacityClinical Use Case
LightFluff pulp only (no SAP)300–500 mLExam tables, procedure protection, short-duration use
ModerateFluff pulp + low SAP ratio600–900 mLStandard incontinence, post-operative recovery, wheelchair protection
HeavyFluff pulp + high SAP ratio1,000–1,500 mLOvernight incontinence, heavy wound drainage, extended immobility
Super / MaximumHigh SAP + structured fluff layers1,500+ mLBariatric patients, critical care, extended-wear applications
Procurement note: SAP granules can absorb 200–300× their own weight in fluid and lock it into a gel structure that does not release under pressure — this is why SAP-enhanced pads maintain a dry surface even under patient weight, while fluff-only pads rewet and contribute to skin maceration.

Layer 4: Tissue Wrap Layer

A second tissue layer wraps the underside of the absorbent core, containing the fluff pulp and SAP granules and preventing particle migration toward the backsheet. This layer also contributes to the structural integrity of the pad when wet.

Layer 5: PE Film Backsheet (Waterproof Barrier)

The backsheet is a polyethylene (PE) film at 20–22 GSM that provides the waterproof barrier protecting the underlying surface. Standard underpads use a blue PE film; premium variants use a cloth-like (SMS nonwoven laminated) backsheet that improves breathability and reduces noise during patient repositioning.

Section 03

Standard Sizes: Imperial and Metric Specifications

Disposable underpads are manufactured in standardized sizes that correspond to specific clinical applications. Specifying the correct size in procurement documents prevents overspend on oversized pads or inadequate coverage from undersized ones.

Size (Imperial)Size (Metric)Typical ApplicationAbsorbent Area Coverage
17 × 24"~43 × 61 cmExam tables, procedure trays, small surface protectionPartial bed coverage
23 × 24"~58 × 61 cmWheelchair seats, recliner chairs, pediatric useChair-width coverage
23 × 36"~58 × 91 cmStandard hospital bed — most common procurement sizeHip-to-shoulder coverage
30 × 30"~76 × 76 cmPost-surgical recovery, lateral positioningWide torso coverage
30 × 36"~76 × 91 cmHeavy incontinence, overnight use, bariatric patientsExtended bed coverage
36 × 36"~91 × 91 cmBariatric / ICU, full-width bed protectionMaximum single-pad coverage
Size selection principle: The 23×36" underpad is the most widely procured size globally because it provides adequate hip-to-shoulder coverage on a standard hospital bed while keeping per-unit cost manageable. For GCC hospital tenders, 60×90 cm is the metric equivalent most frequently specified.
Section 04

Absorbency Testing and Performance Metrics

When evaluating underpad specifications, three performance metrics determine clinical adequacy. These should be included in every procurement RFQ to ensure objective comparison across suppliers:

Total Absorbent Capacity (TAC)

Total volume of fluid the pad can absorb before saturation, measured in milliliters. This is the headline specification but does not tell the full story — a pad with high TAC but slow acquisition rate will pool fluid on the surface before absorbing it.

Rate of Acquisition (ROA)

Speed at which the topsheet transfers fluid into the core, measured as the time (in seconds) for a standard volume of liquid to disappear from the surface. Faster ROA reduces skin contact time with fluid, which is the primary mechanism for preventing incontinence-associated dermatitis (IAD). A well-designed underpad should achieve ROA under 20 seconds for a 100 mL insult.

Rewet / Strike-Through

The amount of fluid that returns to the surface when pressure is applied to a wet pad, measured in grams. This metric directly correlates with SAP content: SAP locks fluid into a gel matrix that resists pressure-release, while fluff-only pads rewet significantly. Specify maximum rewet values in procurement documents — typically under 5 g for heavy-absorbency products.

These three metrics together — TAC, ROA, and rewet — form the performance triangle that procurement managers should require from every supplier quotation. A pad with a 1,200 mL TAC but 10 g rewet is functionally inferior to a pad with 900 mL TAC and 2 g rewet for overnight incontinence use.

Section 05

Clinical Applications and Facility-Specific Selection

Different care settings have different underpad requirements. Standardizing on a single SKU across an entire facility is a common procurement error that leads to either overspend (heavy pads on exam tables) or inadequate protection (light pads for overnight incontinence).

Acute Care / Hospital Wards

Hospital inpatient units typically require moderate-to-heavy absorbency underpads (23×36" or 30×36") for post-surgical patients, wound drainage management, and overnight incontinence. Specify SAP-enhanced cores and low rewet values. Volume procurement in this setting favors bulk packaging (100–300 pads per case).

Intensive Care / Bariatric Units

ICU and bariatric settings demand large-format (30×36" or 36×36") heavy-to-super absorbency pads with reinforced topsheets for patient repositioning. Cloth-like backsheets are preferred in ICU settings to reduce noise during sleep cycles and improve breathability for extended immobility patients.

Nursing Homes / Long-Term Care

Long-term care facilities are the highest-volume consumers of underpads. The economic calculus favors moderate absorbency pads changed at regular intervals over super-absorbency pads changed less frequently — but this calculation must account for nursing time per change and skin integrity outcomes, not just pad cost.

Home Healthcare

Home care procurement prioritizes smaller pack sizes (10–25 per pack), moderate absorbency, and consumer-friendly packaging with clear usage instructions. The 23×36" size dominates home care distribution.

Surgical / OR Settings

Operating room underpads require light-to-moderate absorbency for fluid containment during procedures. In this setting, the primary function is surface protection rather than incontinence management, and pads are single-use with short contact times.

Section 06

Regulatory Standards and Certifications

Disposable underpads are classified as Class I medical devices in most regulatory frameworks. While Class I devices carry the lightest regulatory burden, procurement managers must still verify that suppliers hold the correct certifications for the destination market.

MarketRequired CertificationRegulatory BodyKey Requirement
European UnionCE marking (EU MDR 2017/745)Notified BodyTechnical file, Declaration of Conformity, biocompatibility per ISO 10993
United StatesFDA Registration + 510(k) or ListingFDAEstablishment registration, device listing, labeling requirements
Saudi Arabia / GCCSFDA Medical Device RegistrationSFDARequires CE or FDA as prerequisite; Arabic labeling
Global (QMS)ISO 13485:2016Accredited CBQuality management system for medical device manufacturing
US reimbursement: Disposable underpads are classified under HCPCS code A4554 (Disposable underpads, all sizes) for Medicare / Medicaid reimbursement. Procurement managers sourcing for US healthcare facilities should confirm that the supplier's product labeling aligns with HCPCS classification requirements.

Material-specific standards include ISO 10993 (biological evaluation of medical devices) for biocompatibility testing of the topsheet and any adhesive components, and ISO 11607 for sterile barrier packaging where applicable. Most underpads are sold non-sterile, but surgical-grade variants may require sterile individual packaging.

Section 07

OEM Specification Parameters for Custom Manufacturing

OEM underpad manufacturing allows procurement teams to specify exact parameters across every construction layer. The following checklist covers the specification variables available for custom production:

Topsheet Customization

  • Material: Spunbond PP (standard), spunlace (premium softness), SMS (fluid barrier + softness)
  • GSM: 15–45 GSM range; higher GSM = softer feel, better SAP containment
  • Surface treatment: Hydrophilic coating, antibacterial treatment, quilted pattern (diamond, channel)

Core Customization

  • Fluff pulp grade: Virgin cellulose (standard), chemically modified fluff (improved wicking)
  • SAP content: 0 g (light), 5–15 g (moderate), 15–30 g (heavy), 30+ g (super) per pad
  • Core structure: Homogeneous blend or layered (SAP concentrated in center zone)
  • Total pad weight: 30 g (economy) to 150+ g (super absorbency) per piece

Backsheet Customization

  • Material: PE film (standard, waterproof), cloth-like nonwoven laminate (breathable, quiet)
  • Color: Blue (standard), white, green, custom colors
  • Anti-slip: Textured or adhesive strip options for repositioning-resistant applications

Packaging and Branding

  • Pack count: 5, 10, 20, 25, 50, or 100 per polybag
  • Case count: 100–300 pads per shipping case (standard bulk)
  • Private label: Custom print on polybag, inner box, and outer carton
  • Language: English, Arabic, Spanish, French — per market requirement
Section 08

Procurement Specification Checklist for RFQ / Tender

Use the following specification template when drafting RFQ documents or evaluating supplier quotations for disposable underpads. Every parameter should be explicitly stated to prevent specification ambiguity:

ParameterSpecification to StateExample Value
SizeLength × Width (specify inches or cm)23 × 36" (60 × 90 cm)
Absorbency TierLight / Moderate / Heavy / SuperHeavy
Total Absorbent CapacityMinimum mL capacity≥ 1,200 mL
Core CompositionFluff pulp + SAP (state if SAP required)Fluff pulp + SAP, minimum 15 g SAP/pad
Topsheet MaterialNonwoven type + GSMSpunbond PP, ≥ 22 GSM, hydrophilic
Backsheet MaterialPE film or cloth-likePE film, waterproof, blue
Rewet (Strike-Through)Maximum grams under pressure≤ 5 g
Pad WeightGrams per piece≥ 90 g/pad
SterilitySterile or non-sterileNon-sterile
PackagingPads per polybag, bags per case10/bag, 200/case
CertificationsCE / FDA / ISO 13485 / SFDACE + ISO 13485
Labeling LanguagePer destination marketEnglish + Arabic
Shelf LifeMinimum months from manufacturing≥ 36 months

Request a Certificate of Analysis (CoA) with each shipment confirming absorbent capacity, rewet performance, and biocompatibility test results. For GCC tenders, confirm that the supplier's CoA includes ISO 10993 biocompatibility data and that labeling complies with SFDA Arabic-language requirements.

Source Disposable Underpads with Custom OEM Specifications

Available in all standard sizes · Light to Super absorbency · SAP-enhanced cores · CE & ISO 13485 certified · Private label packaging · Arabic labeling available

Frequently Asked Questions

What is the standard 5-layer construction of a disposable underpad?
A standard disposable underpad consists of five layers: a hydrophilic nonwoven topsheet (15–45 GSM spunbond polypropylene), a tissue acquisition layer, an absorbent core of fluff pulp blended with superabsorbent polymer (SAP), a second tissue wrap layer, and a waterproof polyethylene (PE) film backsheet (20–22 GSM). Each layer serves a specific function in the fluid management chain from acquisition through retention and barrier protection.
What sizes do disposable underpads come in?
Standard imperial sizes include 17×24", 23×24", 23×36", 30×30", 30×36", and 36×36". Metric equivalents include 40×60 cm, 60×60 cm, 60×90 cm, and 80×150 cm. The 23×36" (60×90 cm) size is the most commonly procured for hospital use globally. Custom sizes are available through OEM manufacturing.
How do underpad absorbency levels differ?
Light absorbency underpads use fluff pulp only and hold approximately 300–500 mL — suitable for procedure tables and short-duration use. Moderate absorbency pads combine fluff pulp with SAP for 600–900 mL capacity. Heavy and super absorbency pads use a high SAP-to-fluff ratio and can absorb 1,000–1,500 mL or more, suitable for overnight incontinence and critical care applications.
What certifications should disposable underpads carry for international procurement?
For EU and GCC markets, underpads should carry CE marking under EU MDR 2017/745 (Class I medical device) and ISO 13485 quality management certification. For the US market, FDA registration is required. GCC procurement may additionally require SFDA registration for Saudi Arabia. Biocompatibility testing per ISO 10993 should be confirmed via Certificate of Analysis.
What is the US Medicare reimbursement code for disposable underpads?
Disposable underpads are classified under HCPCS code A4554 (Disposable underpads, all sizes) for US Medicare and Medicaid reimbursement purposes. Procurement managers sourcing for US healthcare facilities should ensure supplier labeling aligns with HCPCS classification requirements.

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