FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Cavilon™

DI: 10707387810693 · Model: 5050 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
3M™ Cavilon™
Primary DI
10707387810693
Version / Model
5050
Catalog Number
5050
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-02
Public Version
1
Public Version Date
2023-06-12
Public Version Status
New
Public Device Record Key
9ec354e9-b2ce-47fe-8173-242c999eb7e4

Device Description

3M™ Cavilon™ Advanced Skin Protectant 5050, 20 EA/Case

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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 50707387810691
Primary 10707387810693

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K153571 000