← Back to catalogue

DuBan®

FDA UDI

Class I (US FDA UDI)

by Derma Sciences Canada, Inc

Identity

Trade Name
DuBan® FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, reusable FDA UDI
Device Name
2 in X 5 yards Cohesive Elastic Bandage. FDA UDI
Model / Reference
73202 FDA UDI
Description
2 in X 5 yards Cohesive Elastic Bandage. FDA UDI

Identifiers

Catalog Number
DUP73202 FDA UDI
Primary DI / UDI-DI
00809958072813 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, reusable 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

No

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: Skin treatment/dressing-supportive limb/finger bandage, reusable

DuBan® by Derma Sciences Canada, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, reusable.

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
Derma Sciences Canada, Inc

Sources (1)

  • FDA UDI 7ae6860c-bf49-48b3-a9ca-78881829cb58 36 fields · synced May 31, 2026