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ProCure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
ProCure FDA UDI
Generic Name
Stockinette FDA UDI
Device Name
Bandages Elastic w/Velcro Self-Closure 6"x 5yds Latex-Free - 10ea/bx 5bx/cs FDA UDI
Model / Reference
PCAB600 FDA UDI
Description
Bandages Elastic w/Velcro Self-Closure 6"x 5yds Latex-Free - 10ea/bx 5bx/cs FDA UDI

Identifiers

Catalog Number
PCAB600 FDA UDI
Primary DI / UDI-DI
10840330701096 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Stockinette 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 5 Yard FDA UDI
Width — 6 Inch FDA UDI

Category: Stockinette

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

Similar devices

Also classified as Stockinette.

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 501ed393-533e-4d0a-95ec-d6ddca79c449 36 fields · synced Jun 8, 2026