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ProCure

FDA UDI

Class U (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
ProCure FDA UDI
Generic Name
Wound hydrogel dressing, antimicrobial FDA UDI
Device Name
ProCure - Calcium Alginate with Silver 4"x8" 5ea/bx 40bx/cs FDA UDI
Model / Reference
PCHCAS48 FDA UDI
Description
ProCure - Calcium Alginate with Silver 4"x8" 5ea/bx 40bx/cs FDA UDI

Identifiers

Catalog Number
PCHCAS48 FDA UDI
Primary DI / UDI-DI
10840330703212 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound hydrogel dressing, antimicrobial FDA UDI

Classification

Device Class
U 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 8 Inch FDA UDI
Width — 4 Inch FDA UDI

Category: Wound hydrogel dressing, antimicrobial

ProCure by Twin Med, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Twin Med, LLC

Sources (1)

  • FDA UDI 77754686-e436-4f8c-a6dd-57e994b6e7b6 37 fields · synced May 31, 2026