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Cutimed®

FDA UDI

Class I (US FDA UDI)

by Bsn Medical, Inc.

Identity

Trade Name
Cutimed® FDA UDI
Generic Name
Synthetic-polymer liquid barrier dressing FDA UDI
Device Name
CUTIMED PROTECT FOAM STERILE 3ML 25 FDA UDI
Model / Reference
72654-03 FDA UDI
Description
CUTIMED PROTECT FOAM STERILE 3ML 25 FDA UDI

Identifiers

Catalog Number
72654-03 FDA UDI
Primary DI / UDI-DI
04042809386448 FDA UDI
FDA Product Code
NEC FDA UDI
GMDN Term
Synthetic-polymer liquid barrier dressing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5090 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

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI

Category: Synthetic-polymer liquid barrier dressing

Cutimed® by Bsn Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic-polymer liquid barrier dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bsn Medical, Inc.

Sources (1)

  • FDA UDI 239c1d6d-b59b-40be-8d9e-f07f3ae88e1e 36 fields · synced Jun 1, 2026