FDA UDI In Commercial Distribution 🇺🇸 United States

Original Posterior Matrix B Series

DI: D94930302125C1 · Model: B302 Clear · Bioclear Matrix Systems
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Original Posterior Matrix B Series
Primary DI
D94930302125C1
Version / Model
B302 Clear
Company Name
Bioclear Matrix Systems
Labeler DUNS
059020838
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2023-09-11
Public Version
1
Public Version Date
2023-09-19
Public Version Status
New
Public Device Record Key
bf6eb5f7-3f9a-413a-841d-a685b4d438b5

Device Description

Clear matrix used in dental restorations.

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JEP Retainer, Matrix

GMDN Terms

Code Name
38786 Dental matrix band, single-use

Identifiers

Type ID
Unit of Use D949303021C0
Primary D94930302125C1