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Cuticell®

FDA UDI

Class I (US FDA UDI)

by Bsn Medical, Inc.

Identity

Trade Name
Cuticell® FDA UDI
Generic Name
Wound-nonadherent dressing, permeable, non-antimicrobial FDA UDI
Device Name
CUTICELL STERILE 7.5CMX20CM 1 FDA UDI
Model / Reference
72539-03 FDA UDI
Description
CUTICELL STERILE 7.5CMX20CM 1 FDA UDI

Identifiers

Catalog Number
72539-03 FDA UDI
Primary DI / UDI-DI
04042809224269 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Wound-nonadherent dressing, permeable, non-antimicrobial 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

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

Dimensions & Sizes

Size
Width — 7.5 Centimeter FDA UDI
Length — 20 Centimeter FDA UDI

Category: Wound-nonadherent dressing, permeable, non-antimicrobial

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

Similar devices

Also classified as Wound-nonadherent dressing, permeable, non-antimicrobial.

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 b361f15a-64b0-4228-8a29-27203860213b 36 fields · synced Jun 8, 2026