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ProCure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
ProCure FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI
Device Name
Unna Boot Bandage 4"x10yds with Zinc 1ea/bx 12/cs FDA UDI
Model / Reference
PCUZ04 FDA UDI
Description
Unna Boot Bandage 4"x10yds with Zinc 1ea/bx 12/cs FDA UDI

Identifiers

Catalog Number
PCUZ04 FDA UDI
Primary DI / UDI-DI
10840330703571 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 4 Inch FDA UDI
Length — 10 Yard FDA UDI

Category: Skin treatment/dressing-supportive limb/finger bandage, single-use

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

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, single-use.

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 749e3dba-c431-4f39-a078-adededd57d53 37 fields · synced May 30, 2026