Primary Device ID | 07290110721756 |
NIH Device Record Key | 06ab323e-592c-41f4-a452-f508642b7abb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TAPERED TITE FIT |
Version Model Number | TFR-16mm |
Catalog Number | TFR-16 |
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 | true |
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 | 07290110721756 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-05-22 |
07290110721800 | DENTAL IMPLANT |
07290110721794 | DENTAL IMPLANT |
07290110721787 | DENTAL IMPLANT |
07290110721770 | DENTAL IMPLANT |
07290110721763 | DENTAL IMPLANT |
07290110721756 | DENTAL IMPLANT |
07290110721749 | DENTAL IMPLANT |
07290110721732 | DENTAL IMPLANT |
07290110721725 | DENTAL IMPLANT |
07290110721718 | DENTAL IMPLANT |
07290110721701 | DENTAL IMPLANT |
07290110721695 | DENTAL IMPLANT |
07290110721688 | DENTAL IMPLANT |
07290110721671 | DENTAL IMPLANT |
07290110721664 | DENTAL IMPLANT |