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Opsite Post-Op Visible 25x10cm Ctn 20

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew Medical, Ltd.

Identity

Trade Name
Opsite Post-Op Visible 25x10cm Ctn 20 FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
Waterproof, bacteria proof dressing with absorbent see through pad FDA UDI
Model / Reference
66800139 FDA UDI
Description
Waterproof, bacteria proof dressing with absorbent see through pad FDA UDI

Identifiers

Catalog Number
66800139 FDA UDI
Primary DI / UDI-DI
05000223463137 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Adhesive bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

Opsite Post-Op Visible 25x10cm Ctn 20 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 7c12557b-9e33-4d64-a86e-1f01d59d53f8 34 fields · synced Jun 1, 2026