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Actibride™

FDA UDI

Class I (US FDA UDI)

by Advanced Medical Solutions Limited

Identity

Trade Name
Actibride™ FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
ActivHeal® Actibride™ Debridement Pad 11cmx18cm FDA UDI
Model / Reference
Debridement Pad FDA UDI
Description
ActivHeal® Actibride™ Debridement Pad 11cmx18cm FDA UDI

Identifiers

Catalog Number
9039169 FDA UDI
Primary DI / UDI-DI
15032749039166 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze pad, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Woven gauze pad, non-antimicrobial

Actibride™ by Advanced Medical Solutions Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Woven gauze pad, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5b27fcad-d527-4051-8f3a-afb7cb2229ea 34 fields · synced May 30, 2026