Primary Device ID | 00810125999772 |
NIH Device Record Key | 83314690-cbfe-4a66-ad4e-375243ed0d7d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET STUD ABUTMENT |
Version Model Number | ETSAO354S |
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 | 00810125999772 [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 | 2024-12-31 |
Device Publish Date | 2024-12-23 |
00810125995514 | ETSA3560C |
00810125995507 | ETSA3550C |
00810125995491 | ETSA3540C |
00810125995484 | ETSA3530C |
00810125995477 | ETSA3520C |
00810125995460 | ETSA3510C |
00810125995453 | ETSAM3560C |
00810125995446 | ETSAM3550C |
00810125995439 | ETSAM3540C |
00810125995422 | ETSAM3530C |
00810125995415 | ETSAM3520C |
00810125995408 | ETSAM3510C |
00810125999819 | ETSAO356S |
00810125999802 | ETSAO356M |
00810125999796 | ETSAO355S |
00810125999789 | ETSAO355M |
00810125999772 | ETSAO354S |
00810125999765 | ETSAO354M |
00810125999758 | ETSAO353S |
00810125999741 | ETSAO353M |
00810125999734 | ETSAO352S |
00810125999727 | ETSAO352M |
00810125999710 | ETSAO351S |
00810125999703 | ETSAO351M |