Primary Device ID | 00810125994319 |
NIH Device Record Key | 9c4c2010-20cb-47c4-82fc-a34470970c8f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET FREEFORM ST ABUTMENT SET |
Version Model Number | ETFA7030CWH |
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 | 00810125994319 [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 | 2024-07-15 |
Device Publish Date | 2024-07-06 |
00810125994364 | ETFAS5030NCWH |
00810125994357 | ETFAS5030CWH |
00810125994340 | ETFAS5015NCWH |
00810125994333 | ETFAS5015CWH |
00810125994326 | ETFA7030NCWH |
00810125994319 | ETFA7030CWH |
00810125994302 | ETFA7015NCWH |
00810125994296 | ETFA7015CWH |
00810125994289 | ETFA6030NCWH |
00810125994272 | ETFA6030CWH |
00810125994265 | ETFA6015NCWH |
00810125994258 | ETFA6015CWH |
00810125994241 | ETFA5030NCWH |
00810125994234 | ETFA5030CWH |
00810125994227 | ETFA5015NCWH |
00810125994210 | ETFA5015CWH |
00810125994203 | ETFA4030NCWH |
00810125994197 | ETFA4030CWH |
00810125994180 | ETFA4015NCWH |
00810125994173 | ETFA4015CWH |
00810125994166 | ETFAM4030NCWH |
00810125994159 | ETFAM4030CWH |
00810125994142 | ETFAM4015NCWH |
00810125994135 | ETFAM4015CWH |