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ReliaTect® Post-Op Dressing with CHG

FDA UDI

Class U (US FDA UDI)

by Avery Dennison Corporation

Identity

Trade Name
ReliaTect® Post-Op Dressing with CHG FDA UDI
Generic Name
Exudate-absorbent dressing, non-gel, antimicrobial FDA UDI
Device Name
ReliaTect® Post-Op Dressing with CHG, Small, 3.2 x 5.9 in (8 x 15 cm) FDA UDI
Model / Reference
0496-0567-76 FDA UDI
Description
ReliaTect® Post-Op Dressing with CHG, Small, 3.2 x 5.9 in (8 x 15 cm) FDA UDI

Identifiers

Primary DI / UDI-DI
00817138010500 FDA UDI
510(k) Number
K163529 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Exudate-absorbent dressing, non-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

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

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

ReliaTect® Post-Op Dressing with CHG by Avery Dennison Corporation — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K163529 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avery Dennison Corporation

Sources (1)

  • FDA UDI 843f5716-67ed-4254-b0ab-c8eefe498c32 34 fields · synced May 31, 2026