FDA UDI In Commercial Distribution 🇺🇸 United States

3M™

DI: 04035077005333 · Model: 56940 · 3M Deutschland GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

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Basic Information

Brand Name
3M™
Primary DI
04035077005333
Version / Model
56940
Catalog Number
56940
Company Name
3M Deutschland GmbH
Labeler DUNS
315731711
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2017-08-04
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
5cb1be9a-b2a1-449b-acbc-6cdaf9e0c955

Device Description

3M™ ESPE™ Retraction Capsule Sample Kit, 56940

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 04035077005333
Unit of Use 44035077005331

Customer Contacts