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Cosmopor Steril 7.2x5cm P50 C20

FDA UDI

Class I (US FDA UDI)

by Paul Hartmann Corp.

Identity

Trade Name
Cosmopor Steril 7.2x5cm P50 C20 FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
Cosmopor Steril 7.2x5cm P50 C20 FDA UDI
Model / Reference
900800 Cosmopor Steril 7.2x5cm P50 C20 FDA UDI
Description
Cosmopor Steril 7.2x5cm P50 C20 FDA UDI

Identifiers

Primary DI / UDI-DI
04049500217484 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

Yes

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

Yes

FDA UDI

Category: Adhesive bandage

Cosmopor Steril 7.2x5cm P50 C20 by Paul Hartmann Corp. — 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

Manufacturer
Paul Hartmann Corp.

Sources (1)

  • FDA UDI aaac6ce5-543e-4d17-ac3d-b76a0d8ad0f2 33 fields · synced May 30, 2026