TI-OSS

GUDID 08809490620444

CHIYEWON.LTD

Dental bone matrix implant, animal-derived
Primary Device ID08809490620444
NIH Device Record Key9529fe41-4adb-45e6-96ce-6b2a76679391
Commercial Distribution StatusIn Commercial Distribution
Brand NameTI-OSS
Version Model Number20-1217
Company DUNS689846859
Company NameCHIYEWON.LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108809490620444 [Primary]

FDA Product Code

NPMBone Grafting Material, Animal Source

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-11-04
Device Publish Date2016-06-13

On-Brand Devices [TI-OSS]

08809490620567S05-1217
08809490620550S25-1217
08809490620505S05-0512
08809490620499S25-0512
0880949062044420-1217
0880949062043710-1217
0880949062042005-1217
0880949062041325-1217
0880949062029120-0512
0880949062028410-0512
0880949062027705-0512
0880949062026025-0512
0880949062014720-0210
0880949062013010-0210
0880949062012305-0210
0880949062011625-0210

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