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ProCure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
ProCure FDA UDI
Generic Name
Dressing-fixation skin adhesive tape, non-silicone FDA UDI
Device Name
Tape Paper 2" Hypoallergenic Latex Free - 6ea/bx 12bx/cs FDA UDI
Model / Reference
PCTP20 FDA UDI
Description
Tape Paper 2" Hypoallergenic Latex Free - 6ea/bx 12bx/cs FDA UDI

Identifiers

Catalog Number
PCTP20 FDA UDI
Primary DI / UDI-DI
10840330700884 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Dressing-fixation skin adhesive tape, non-silicone FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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
Width — 2 Inch FDA UDI

Category: Dressing-fixation skin adhesive tape, non-silicone

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

Similar devices

Also classified as Dressing-fixation skin adhesive tape, non-silicone.

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 8a820b26-919b-418b-9b9d-d41dd275ab9d 36 fields · synced Jun 1, 2026