Primary Device ID | 07290110723972 |
NIH Device Record Key | b35a96a7-c724-425a-9550-069aa388dceb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SELF THREAD /LOGIC PLUS/SPARK |
Version Model Number | ACA-S |
Catalog Number | ACA-S |
Company DUNS | 600710917 |
Company Name | HI-TEC IMPLANTS 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 | 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 | 07290110723972 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2017-06-08 |
07290110728564 | ABUTMENT SCREW |
07290110728557 | ABUTMENT SCREW |
07290110728540 | TRANSFER SCREW |
07290110728533 | TRANSFER SCREW |
07290110728526 | ABUTMENT SCREW |
07290110728519 | ABUTMENT SCREW |
07290110728502 | ABUTMENT SCREW |
07290110723996 | ANTI-ROTATION ABUTMENT |
07290110723989 | ANTI-ROTATION ABUTMENT |
07290110723972 | ANTI-ROTATION ABUTMENT |
07290110723965 | ANTI-ROTATION ABUTMENT |
07290110723958 | ANTI-ROTATION ABUTMENT |
07290110723941 | ANTI-ROTATION ABUTMENT |
07290110723934 | ANTI-ROTATION ABUTMENT |
07290110723927 | ANTI-ROTATION ABUTMENT |