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kerraFoam Gentle Border

FDA UDI

Class I (US FDA UDI)

by Crawford Healthcare Limited

Identity

Trade Name
kerraFoam Gentle Border FDA UDI
Generic Name
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI
Model / Reference
6.7 x 6.9in FDA UDI

Identifiers

Catalog Number
CWL1023 FDA UDI
Primary DI / UDI-DI
05060077230996 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 6.9 Inch FDA UDI
Height — 6.7 Inch FDA UDI

Category: Exudate-absorbent dressing, non-gel, non-antimicrobial

kerraFoam Gentle Border by Crawford Healthcare Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, non-gel, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dafd3c0f-72df-40fa-8251-78592ed0ac0d 36 fields · synced Jun 7, 2026