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carePAC

FDA UDI

Class II (US FDA UDI)

by Extremity Care, Llc

Identity

Trade Name
carePAC FDA UDI
Generic Name
Wound dressing kit, medicated FDA UDI
Device Name
Daily carePAC Collagen Matrix 30PAC FDA UDI
Model / Reference
ECD-030 FDA UDI
Description
Daily carePAC Collagen Matrix 30PAC FDA UDI

Identifiers

Primary DI / UDI-DI
00850003042176 FDA UDI
FDA Product Code
MCY FDA UDI
GMDN Term
Wound dressing kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Wound dressing kit, medicated

carePAC by Extremity Care, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound dressing kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Extremity Care, Llc

Sources (1)

  • FDA UDI 145d2dc1-7f12-4e9b-bd03-5a110ac10dd9 35 fields · synced May 30, 2026