Primary Device ID | 06947600317975 |
NIH Device Record Key | 8543f8e4-a0b0-40c0-9830-51b954294681 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Implant, Regular |
Version Model Number | 316040G |
Company DUNS | 527603266 |
Company Name | BIO CONCEPT CO.,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 | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06947600317975 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-29 |
Device Publish Date | 2024-11-21 |
06947600317999 | 316060G |
06947600317982 | 316050G |
06947600317975 | 316040G |
06947600317968 | 316030G |
06947600317951 | 316020G |
06947600317944 | 315060G |
06947600317937 | 315050G |
06947600317920 | 315040G |
06947600317913 | 315030G |
06947600317906 | 315020G |
06947600314967 | 314070G |
06947600314950 | 314060G |
06947600314943 | 314050G |
06947600314936 | 314040G |
06947600314929 | 314030G |
06947600314912 | 314020G |
06947600314905 | 313060G |
06947600314899 | 313050G |
06947600314882 | 313040G |
06947600314875 | 313030G |
06947600314868 | 313020G |
06947600314851 | 313010G |
06947600314844 | 312060G |
06947600314837 | 312020G |
06947600314820 | 312010G |
06947600314776 | 312050G |
06947600314721 | 312040G |
06947600314714 | 312030G |