Gutta Percha 04-LM-20

GUDID 08806387808923

Gutta Percha Points and Bars 04 taper #20, 60Points, P31R

Meta Biomed Co., Ltd.

Synthetic gutta-percha
Primary Device ID08806387808923
NIH Device Record Keyc8c56650-a3a2-4da2-ade5-b0f26b75853a
Commercial Distribution StatusIn Commercial Distribution
Brand NameGutta Percha 04-LM-20
Version Model Number0892
Company DUNS688322841
Company NameMeta Biomed Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108806387808923 [Primary]

FDA Product Code

EKMGutta-Percha

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-10
Device Publish Date2021-06-02

On-Brand Devices [Gutta Percha 04-LM-20]

08806387808923Gutta Percha Points and Bars 04 taper #20, 60Points, P31R
08806387807742Gutta Percha Points and Bars 04 taper #20, 60Points, P31S
08806387806110Gutta Percha Points and Bars 04 taper #20, 120Points, P71
08806387804994Gutta Percha Points and Bars 04 taper #20, 60Points, P71
08806387805601Gutta Percha Points and Bars, Length Marked 04 Taper 20, Aurum Blue T1, 60 Points, P 71

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