Primary Device ID | 08800026100867 |
NIH Device Record Key | 4f167ca2-15b9-456f-9097-07b8ae011164 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IU Fixture |
Version Model Number | FIU40070 |
Company DUNS | 688857820 |
Company Name | WARANTEC.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 | 08800026100867 [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 | 2023-04-20 |
Device Publish Date | 2023-04-12 |
08800026101086 | FIU60100 |
08800026101079 | FIU60085 |
08800026101062 | FIU60070 |
08800026101055 | FIU55130 |
08800026101048 | FIU55115 |
08800026101031 | FIU55100 |
08800026101024 | FIU55085 |
08800026101017 | FIU55070 |
08800026101000 | FIU50130 |
08800026100997 | FIU50115 |
08800026100980 | FIU50100 |
08800026100973 | FIU50085 |
08800026100966 | FIU50070 |
08800026100959 | FIU45130 |
08800026100942 | FIU45115 |
08800026100935 | FIU45100 |
08800026100928 | FIU45085 |
08800026100911 | FIU45070 |
08800026100904 | FIU40130 |
08800026100898 | FIU40115 |
08800026100881 | FIU40100 |
08800026100874 | FIU40085 |
08800026100867 | FIU40070 |
08800026100850 | FIU36130 |
08800026100843 | FIU36115 |
08800026100836 | FIU36100 |
08800026100829 | FIU36085 |