FDA UDI In Commercial Distribution 🇺🇸 United States

MU Lab Analog

DI: 08800053039154 · Model: DMLA · DENTIS CO. ,LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MU Lab Analog
Primary DI
08800053039154
Version / Model
DMLA
Company Name
DENTIS CO. ,LTD
Labeler DUNS
694721181
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-01
Public Version
1
Public Version Date
2021-06-09
Public Version Status
New
Public Device Record Key
e0b7e07c-39ae-4894-bb0e-6828b697ebcd

Device Description

Dental Implant Instrument / MU Lab Analog

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
61642 Dental implant analog

Identifiers

Type ID
Primary 08800053039154