Primary Device ID | 07290110720100 |
NIH Device Record Key | 021fca4f-63e3-45b0-a9de-927072714d61 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TAPERED SELF THREAD |
Version Model Number | SLT-16mmSR |
Catalog Number | SLT-16SR |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290110720100 [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 |
07290110720209 | DENTAL IMPLANT |
07290110720193 | DENTAL IMPLANT |
07290110720186 | DENTAL IMPLANT |
07290110720179 | DENTAL IMPLANT |
07290110720162 | DENTAL IMPLANT |
07290110720155 | DENTAL IMPLANT |
07290110720148 | DENTAL IMPLANT |
07290110720131 | DENTAL IMPLANT |
07290110720124 | DENTAL IMPLANT |
07290110720117 | DENTAL IMPLANT |
07290110720100 | DENTAL IMPLANT |
07290110720094 | DENTAL IMPLANT |
07290110720087 | DENTAL IMPLANT |
07290110720070 | DENTAL IMPLANT |
07290110720063 | SLT-8mmSR |
07290110720056 | NTI-16mmSR |
07290110720049 | NTI-13mmSR |
07290110720032 | NTI-11.5mmSR |
07290110720025 | NTI-10mmSR |
07290110720018 | NTI-8mmSR |