FDA UDI In Commercial Distribution 🇺🇸 United States

Imprint™ 4 Preliminary

DI: 04035077008723 · Model: 71539 · 3M Deutschland GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Imprint™ 4 Preliminary
Primary DI
04035077008723
Version / Model
71539
Catalog Number
71539
Company Name
3M Deutschland GmbH
Labeler DUNS
315731711
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2017-08-04
Public Version
3
Public Version Date
2018-12-07
Public Version Status
Update
Public Device Record Key
83e2e329-c066-4681-a90b-9f0b9b144d7c

Device Description

3M™ ESPE™ Imprint™ 4 Regular VPS Preliminary Impression Material Economy Pack, 10 - 50 ml Cartridges, 71539 DM DI = 04035077018760

Device Characteristics

Single Use
No
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
ELW MATERIAL, IMPRESSION

GMDN Terms

Code Name
35866 Silicone dental impression material

Identifiers

Type ID
Primary 04035077008723
Unit of Use 04035077018760

Customer Contacts