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Biatain Fiber Ag

FDA UDI

Class U (US FDA UDI)

by Coloplast A/S

Identity

Trade Name
Biatain Fiber Ag FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial FDA UDI
Model / Reference
33578 FDA UDI

Identifiers

Catalog Number
33578 FDA UDI
Primary DI / UDI-DI
05708932764629 FDA UDI
510(k) Number
K231953 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Width — 20 Centimeter FDA UDI
Length — 30 Centimeter FDA UDI
Length — 12 Inch FDA UDI
Width — 8 Inch FDA UDI

Category: Exudate-absorbent dressing, hydrophilic-gel, antimicrobial

Biatain Fiber Ag by Coloplast A/S — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, hydrophilic-gel, antimicrobial.

Cleared under the same submission

K231953 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Coloplast A/S

Sources (1)

  • FDA UDI 847d4524-3de5-4fef-ac9d-ab7507efdd5b 37 fields · synced May 30, 2026