KerraPro

FDA UDI

Class I (US FDA UDI)

by Crawford Healthcare Limited

Identity

Trade Name: KerraPro FDA UDI
Generic Name: Pressure-management bandage, silicone FDA UDI
Model / Reference: 4 x 4 x 0.5in FDA UDI

Identifiers

Catalog Number: KPRO20 FDA UDI
Primary DI / UDI-DI: 05060077230446 FDA UDI
FDA Product Code: FMP FDA UDI
GMDN Term: Pressure-management bandage, silicone FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6450 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Depth — 0.5 Inch FDA UDI
Length — 4 Inch FDA UDI
Height — 4 Inch FDA UDI

Category: Pressure-management bandage, silicone

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Crawford Healthcare Limited

Sources (1)

FDA UDI dcf26d5d-235c-4621-a6e8-fc0b27181e64 35 fields · synced Jun 8, 2026