FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Cavilon™

DI: 00707387809669 · Model: 3342K · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

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Basic Information

Brand Name
3M™ Cavilon™
Primary DI
00707387809669
Version / Model
3342K
Catalog Number
3342K
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-06-08
Public Version
2
Public Version Date
2026-03-30
Public Version Status
Update
Public Device Record Key
af00a5cb-17e8-4d2d-80f1-80fcc547e1dc

Device Description

FREE_FROM_LATEX

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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMF Bandage, liquid

GMDN Terms

Code Name
58978 Synthetic-polymer liquid barrier dressing

Identifiers

Type ID
Package 50707387809664
Primary 00707387809669
Unit of Use 00707387809652

Customer Contacts