FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Coban™

DI: 04046719703197 · Model: 20714 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
3M™ Coban™
Primary DI
04046719703197
Version / Model
20714
Catalog Number
20714
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-21
Public Version
1
Public Version Date
2026-04-29
Public Version Status
New
Public Device Record Key
43a28408-bd21-48d3-96df-e584639661ea

Device Description

3M™ Coban™ 2 Lite Comfort Foam Layer, 20714, 18/Carton, 2 Cartons/Case

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FQM BANDAGE, ELASTIC

GMDN Terms

Code Name
58983 Compression bandaging kit

Identifiers

Type ID
Package 04046719713813
Primary 04046719703197

Customer Contacts