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Zorflex

FDA UDI

Class I (US FDA UDI)

by Chemviron Carbon Limited

Identity

Trade Name
Zorflex FDA UDI
Generic Name
Odour-absorbent dressing, antimicrobial FDA UDI
Device Name
Odor adsorbing medical wound dressing consisting of cut pieces of activated carbon cloth FDA UDI
Model / Reference
ZF20 FDA UDI
Description
Odor adsorbing medical wound dressing consisting of cut pieces of activated carbon cloth FDA UDI

Identifiers

Catalog Number
ZF20 FDA UDI
Primary DI / UDI-DI
05060467570145 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Odour-absorbent dressing, antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 20 Centimeter FDA UDI
Width — 10 Centimeter FDA UDI

Category: Odour-absorbent dressing, antimicrobial

Zorflex by Chemviron Carbon Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Odour-absorbent dressing, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Chemviron Carbon Limited

Sources (1)

  • FDA UDI 32b5e390-c490-43c5-aea2-7cc61074716d 37 fields · synced May 30, 2026