← Back to catalogue

3M™ Coban™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Coban™ FDA UDI
Generic Name
Pressure bandage, Hevea-latex, single-use FDA UDI
Device Name
3M™ Coban™ Self-Adherent Wrap, 1586S, Sterile, 6 in x 5 yd (15 cm x 4,5 m), 12 Rolls/Case FDA UDI
Model / Reference
1586S FDA UDI
Description
3M™ Coban™ Self-Adherent Wrap, 1586S, Sterile, 6 in x 5 yd (15 cm x 4,5 m), 12 Rolls/Case FDA UDI

Identifiers

Catalog Number
1586S FDA UDI
Primary DI / UDI-DI
00707387802301 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure bandage, Hevea-latex, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pressure bandage, Hevea-latex, single-use

3M™ Coban™ by 3m Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, Hevea-latex, single-use.

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
3m Company

Sources (1)

  • FDA UDI afe9226c-582a-4115-a3e7-9a86cb64dfc1 35 fields · synced Jun 8, 2026