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Exufiber® Ag+

FDA UDI

Class U (US FDA UDI)

by Mölnlycke Health Care AB

Identity

Trade Name
Exufiber® Ag+ FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial FDA UDI
Device Name
Exufiber Ag+ 4x4.8" (10x12cm) FDA UDI
Model / Reference
603422 FDA UDI
Description
Exufiber Ag+ 4x4.8" (10x12cm) FDA UDI

Identifiers

Primary DI / UDI-DI
07323190161010 FDA UDI
510(k) Number
K160379 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Exufiber® Ag+ by Mölnlycke Health Care AB — 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

K160379 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mölnlycke Health Care AB

Sources (1)

  • FDA UDI 64f3df1b-7d85-4f6d-b1c7-3dc6eb30f578 36 fields · synced Jun 1, 2026