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CotZee

FDA UDI

Class I (US FDA UDI)

by Hemasource

Identity

Trade Name
CotZee FDA UDI
Generic Name
Non-adhesive device retention bandage FDA UDI
Device Name
CotZee Cohesive Bandage 2" x 5 Yds. LF WHITE FDA UDI
Model / Reference
CZ20LFPW FDA UDI
Description
CotZee Cohesive Bandage 2" x 5 Yds. LF WHITE FDA UDI

Identifiers

Primary DI / UDI-DI
00891153001330 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Non-adhesive device retention bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-adhesive device retention bandage

CotZee by Hemasource — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-adhesive device retention bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hemasource

Sources (1)

  • FDA UDI 6de24bcb-6406-4cb7-8110-d62d1a7591ec 33 fields · synced May 30, 2026