Hydrofilm Plus 5x7, 2cm st P50 C10

FDA UDI

Class I (US FDA UDI)

by Paul Hartmann Corp.

Identity

Trade Name: Hydrofilm Plus 5x7,2cm st P50 C10 FDA UDI
Generic Name: Adhesive bandage FDA UDI
Device Name: Hydrofilm Plus 5x7,2cm st P50 C10 FDA UDI
Model / Reference: 685771 Hydrofilm Plus 5x7,2cm st P50 C10 FDA UDI
Description: Hydrofilm Plus 5x7,2cm st P50 C10 FDA UDI

Identifiers

Primary DI / UDI-DI: 04049500631204 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

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

Yes

FDA UDI

Category: Adhesive bandage

Hydrofilm Plus 5x7, 2cm st P50 C10 by Paul Hartmann Corp. — 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: Paul Hartmann Corp.

Sources (1)

FDA UDI 24abc4e1-bca8-49ba-bc82-bb314591e878 33 fields · synced Jun 1, 2026