FDA UDI In Commercial Distribution 🇺🇸 United States

Lava™

DI: J001702011448080 · Model: 69154 · 3M Deutschland GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
Lava™
Primary DI
J001702011448080
Version / Model
69154
Catalog Number
69154
Company Name
3M Deutschland GmbH
Labeler DUNS
315731711
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
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
8869a1ae-f76f-46c6-9834-4785244fb268

Device Description

3M™ ESPE™ Lava™ Ultimate Restorative S - A1-LT, 69154A1-LT, 69154

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
EBF MATERIAL, TOOTH SHADE, RESIN

GMDN Terms

Code Name
38649 Resin dental inlay

Identifiers

Type ID
Primary J001702011448080
Unit of Use J001702011448084

Customer Contacts