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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
20 x 1 x 0.1in FDA UDI

Identifiers

Catalog Number
KPRO60 FDA UDI
Primary DI / UDI-DI
05060077230637 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

No

FDA UDI

Single Use

No

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

Category: Pressure-management bandage, silicone

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

Similar devices

Also classified as Pressure-management bandage, silicone.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7898ae0-6391-49be-91ae-f17d9a1c149d 34 fields · synced May 30, 2026