Diamond Wedge Kit

GUDID D9498120042

Convenience kit of Bioclear products used in dental restorations.

Bioclear Matrix Systems

Dental wedge, single-use
Primary Device IDD9498120042
NIH Device Record Keyeb25bec2-cc0e-4cd8-b8b5-5a4a09bfd98c
Commercial Distribution StatusIn Commercial Distribution
Brand NameDiamond Wedge Kit
Version Model NumberOriginal Assorted 8ct
Company DUNS059020838
Company NameBioclear Matrix Systems
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD9498120042 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-19
Device Publish Date2023-09-11

On-Brand Devices [Diamond Wedge Kit]

D9498120072Convenience kit of Bioclear products used in dental restorations.
D9498120012Convenience kit of Bioclear products used in dental restorations.
D9498120042Convenience kit of Bioclear products used in dental restorations.
D9498120013Convenience kit of Bioclear products used in dental restorations.

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.