Primary Device ID | 08800020854896 |
NIH Device Record Key | 24ba32a5-4c2e-4f02-8968-11ebab5596c5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SNUCONE BONE LEVEL IMPLANT SYSTEM |
Version Model Number | AF+B-6807S |
Company DUNS | 688806132 |
Company Name | SNUCONE Co.,LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com | |
Phone | 9999999999 |
snucone@naver.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800020854896 [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 | 2023-02-22 |
Device Publish Date | 2023-02-14 |