Primary Device ID | 00810019240805 |
NIH Device Record Key | b031bd3e-0c19-4404-a073-db2d9038e6eb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET FREEFORM ST ABUTMENT |
Version Model Number | ETFSA401SNW |
Company DUNS | 796083090 |
Company Name | HIOSSEN, INC. |
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 | false |
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 | 00810019240805 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-23 |
Device Publish Date | 2019-05-15 |
00810019240980 | ETFSA703SNW |
00810019240973 | ETFSA703SHW |
00810019240966 | ETFSA701SNW |
00810019240959 | ETFSA701SHW |
00810019240942 | ETFSA603SNW |
00810019240935 | ETFSA603SHW |
00810019240928 | ETFSA601SNW |
00810019240911 | ETFSA601SHW |
00810019240904 | ETFSA503SNW |
00810019240898 | ETFSA503SHW |
00810019240881 | ETFSA501SNW |
00810019240874 | ETFSA501SHW |
00810019240867 | ETFSAS503SNW |
00810019240850 | ETFSAS503SHW |
00810019240843 | ETFSAS501SNW |
00810019240836 | ETFSAS501SHW |
00810019240829 | ETFSA403SNW |
00810019240812 | ETFSA403SHW |
00810019240805 | ETFSA401SNW |
00810019240799 | ETFSA401SHW |
00810019240782 | ETFSA403MNW |
00810019240775 | ETFSA403MHW |
00810019240768 | ETFSA401MNW |
00810019240751 | ETFSA401MHW |