← Back to catalogue

Endure

FDA UDI

Class I (US FDA UDI)

by Endure Industries, Inc.

Identity

Trade Name
Endure FDA UDI
Generic Name
Hypoallergenic skin adhesive tape FDA UDI
Device Name
Surgical Tape, Breathable, Tan, 2" x 10 yd FDA UDI
Model / Reference
ST21A3-0520 FDA UDI
Description
Surgical Tape, Breathable, Tan, 2" x 10 yd FDA UDI

Identifiers

Catalog Number
ST21A3 FDA UDI
Primary DI / UDI-DI
00840118601412 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Hypoallergenic skin adhesive tape 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 2 Inch FDA UDI
Length — 10 Yard FDA UDI

Category: Hypoallergenic skin adhesive tape

Endure by Endure Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hypoallergenic skin adhesive tape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1361644a-d1ac-430d-a315-b3a897d44702 37 fields · synced Jun 8, 2026