FDA UDI In Commercial Distribution 🇺🇸 United States

MANI DIA-BURS

DI: 04546951609443 · Model: FO-33F · MANI, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
MANI DIA-BURS
Primary DI
04546951609443
Version / Model
FO-33F
Company Name
MANI, INC.
Labeler DUNS
690622428
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2022-12-10
Public Version
1
Public Version Date
2022-12-19
Public Version Status
New
Public Device Record Key
702eaada-ced2-4e62-a75e-555a60e8316a

Device Description

MANI DIA-BURS

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
DZP INSTRUMENT, DIAMOND, DENTAL

GMDN Terms

Code Name
16670 Diamond dental bur, reusable

Identifiers

Type ID
Unit of Use 74546951609442
Primary 04546951609443