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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
Stockinette Tubular 3"x25yd Roll - 6ea/cs FDA UDI
Model / Reference
PCTB300 FDA UDI
Description
Stockinette Tubular 3"x25yd Roll - 6ea/cs FDA UDI

Identifiers

Catalog Number
PCTB300 FDA UDI
Primary DI / UDI-DI
10840330701034 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 — 25 Yard FDA UDI
Width — 3 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 cc380ed1-e7f7-4a2b-9c2d-faff9f1c0e38 36 fields · synced May 31, 2026