FDA UDI In Commercial Distribution 🇺🇸 United States

3M™

DI: J001702011373150 · Model: 56942 · 3M Deutschland GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
3M™
Primary DI
J001702011373150
Version / Model
56942
Catalog Number
56942
Company Name
3M Deutschland GmbH
Labeler DUNS
315731711
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
38ea8936-7af2-454b-ac14-85a7835bc14c

Device Description

3M™ ESPE™ Retraction Capsule Value Pack, 56942

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
MVL CORD, RETRACTION

GMDN Terms

Code Name
16352 Gingival retraction kit

Identifiers

Type ID
Primary J001702011373150
Unit of Use J001702011373154

Customer Contacts