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All Terrain

FDA UDI

Class I (US FDA UDI)

by Rosemont Ventures, Inc.

Identity

Trade Name
ALL TERRAIN FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
Self-Stick Tape, 1 roll, 2 in x 5 yds. (50 mm x 4.5 m) stretched, 2 in x 2.2 yds. (50 mm x 2 m) unstretched FDA UDI
Model / Reference
608503050098 FDA UDI
Description
Self-Stick Tape, 1 roll, 2 in x 5 yds. (50 mm x 4.5 m) stretched, 2 in x 2.2 yds. (50 mm x 2 m) unstretched FDA UDI

Identifiers

Primary DI / UDI-DI
00608503050098 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure bandage, non-latex, 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

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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pressure bandage, non-latex, single-use

All Terrain by Rosemont Ventures, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, non-latex, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8106ce74-b435-4fed-b6b1-87ff4c69803e 33 fields · synced Jun 8, 2026