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Ren/Asys Adhesive Gel Patch

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew Medical, Ltd.

Identity

Trade Name
REN/ASYS ADHESIVE GEL PATCH FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
RENASYS ADHESIVE GEL PATCH FDA UDI
Model / Reference
66801082 FDA UDI
Description
RENASYS ADHESIVE GEL PATCH FDA UDI

Identifiers

Catalog Number
66801082 FDA UDI
Primary DI / UDI-DI
00040565125954 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Adhesive bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

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: Adhesive bandage

Ren/Asys Adhesive Gel Patch by Smith & Nephew Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Adhesive bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cd3562cc-ac09-4274-95cc-63af6522ad72 34 fields · synced May 30, 2026