Primapore Adhesive Dressing 20*10cm

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew Medical, Ltd.

Identity

Trade Name: PRIMAPORE ADHESIVE DRESSING 20*10CM FDA UDI
Generic Name: Adhesive bandage FDA UDI
Device Name: Non-woven adhesive wound dressing FDA UDI
Model / Reference: 66000319 FDA UDI
Description: Non-woven adhesive wound dressing FDA UDI

Identifiers

Catalog Number: 66000319 FDA UDI
Primary DI / UDI-DI: 05000223420284 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Adhesive bandage

Primapore Adhesive Dressing 20*10cm by Smith & Nephew Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Smith & Nephew Medical, Ltd.

Sources (1)

FDA UDI bffc41ad-755b-4d28-8901-b74e323e5cf3 34 fields · synced Jun 8, 2026