← Back to catalogue

Cutimed® Sorbact®

FDA UDI

Class U (US FDA UDI)

by Bsn Medical, Inc.

Identity

Trade Name
Cutimed® Sorbact® FDA UDI
Generic Name
Microbe-binding hydrophobic dressing FDA UDI
Device Name
CUTIMED SORBACT SWABS STERILE 4X6CM 5 US FDA UDI
Model / Reference
72164-13 FDA UDI
Description
CUTIMED SORBACT SWABS STERILE 4X6CM 5 US FDA UDI

Identifiers

Catalog Number
72164-13 FDA UDI
Primary DI / UDI-DI
04042809657449 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Microbe-binding hydrophobic dressing FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Width — 4 Centimeter FDA UDI
Length — 6 Centimeter FDA UDI

Category: Microbe-binding hydrophobic dressing

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

Similar devices

Also classified as Microbe-binding hydrophobic dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bsn Medical, Inc.

Sources (1)

  • FDA UDI 274fefa0-26df-4887-9f90-09e0d3edff93 36 fields · synced Jun 8, 2026