| Primary Device ID | 07290112280145 |
| NIH Device Record Key | 03a4c997-6477-4ba5-8ae3-ce6ba3884f34 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Custom Abutment |
| Version Model Number | CA-100 |
| Company DUNS | 514897185 |
| Company Name | DENTACK 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 | true |
| OTC Over-The-Counter | false |
| Phone | +97297660379 |
| info@pyramidion-is.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290112280145 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07290112280145]
Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2018-02-23 |
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| 07290112280718 - Straight MU Abutment | 2019-03-11 Straight MU Abutment |