FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Cavilon™

DI: 30707387766321 · Model: 3342 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
3M™ Cavilon™
Primary DI
30707387766321
Version / Model
3342
Catalog Number
3342
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2018-09-24
Public Version
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
11707d22-edaa-43f7-bdbb-adacc2a6c8f0

Device Description

3M™ Cavilon™ No Sting Barrie Film 50 Wipes/Carton 8 Cartons/Case 3342

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
No
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
58979 Synthetic-polymer liquid barrier dressing, sterile

Identifiers

Type ID
Package 50707387766325
Primary 30707387766321
Unit of Use 00707387766320

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K955103 000