Primary Device ID | 08809490620116 |
NIH Device Record Key | 0cf2b98a-7c4a-4431-81b3-79c811e26ce1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TI-OSS |
Version Model Number | 25-0210 |
Company DUNS | 689846859 |
Company Name | CHIYEWON.LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809490620116 [Primary] |
NPM | Bone Grafting Material, Animal Source |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-04 |
Device Publish Date | 2016-06-13 |
08809490620567 | S05-1217 |
08809490620550 | S25-1217 |
08809490620505 | S05-0512 |
08809490620499 | S25-0512 |
08809490620444 | 20-1217 |
08809490620437 | 10-1217 |
08809490620420 | 05-1217 |
08809490620413 | 25-1217 |
08809490620291 | 20-0512 |
08809490620284 | 10-0512 |
08809490620277 | 05-0512 |
08809490620260 | 25-0512 |
08809490620147 | 20-0210 |
08809490620130 | 10-0210 |
08809490620123 | 05-0210 |
08809490620116 | 25-0210 |