Primary Device ID | 07290110720483 |
NIH Device Record Key | 08ef7a47-c0e4-4b7d-a293-44c053e172bb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SPARK |
Version Model Number | TPI 4.3-8mm |
Catalog Number | TPI 4.3-8 |
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 | 07290110720483 [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 |
07290110722265 | DENTAL IMPLANT |
07290110720636 | DENTAL IMPLANT |
07290110720629 | DENTAL IMPLANT |
07290110720612 | DENTAL IMPLANT |
07290110720605 | DENTAL IMPLANT |
07290110720599 | DENTAL IMPLANT |
07290110720582 | DENTAL IMPLANT |
07290110720575 | DENTAL IMPLANT |
07290110720568 | DENTAL IMPLANT |
07290110720551 | DENTAL IMPLANT |
07290110720544 | DENTAL IMPLANT |
07290110720537 | DENTAL IMPLANT |
07290110720520 | DENTAL IMPLANT |
07290110720513 | DENTAL IMPLANT |
07290110720506 | DENTAL IMPLANT |
07290110720490 | DENTAL IMPLANT |
07290110720483 | DENTAL IMPLANT |
07290110720476 | DENTAL IMPLANT |
07290110720469 | DENTAL IMPLANT |
07290110720452 | DENTAL IMPLANT |
07290110720445 | DENTAL IMPLANT |
07290110720438 | DENTAL IMPLANT |