FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Coban™

DI: 04046719510665 · Model: 20096 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
3M™ Coban™
Primary DI
04046719510665
Version / Model
20096
Catalog Number
20096
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
61490556-b811-4d67-9b50-463cddf8da7c

Device Description

3M™ Coban™ 2 Two-Layer Compression System 20096, 6", 1 KT/CAR, 8 CAR/CS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
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
Primary 04046719510665

Customer Contacts