| Primary Device ID | 07290117524022 |
| NIH Device Record Key | 8205db56-9001-43d7-bf32-5b97059821be |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tixel Periorbital Handpiece |
| Version Model Number | TPH00001 |
| Catalog Number | TPH00001 |
| Company DUNS | 600275858 |
| Company Name | NOVOXEL LTD |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Lot Batch | true |
| Serial Number | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290117524022 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-11-01 |
| Device Publish Date | 2021-10-24 |
| 07290117524039 - Tixel 2 | 2024-05-31 |
| 07290117524046 - Tixel C | 2021-11-22 |
| 07290117524053 - Tixel Handpiece | 2021-11-22 To be used with Tixel C Model MSTX0002 |
| 07290117524060 - Tixel-Small Tip Handpiece | 2021-11-22 To be used with Tixel C MSTX0002 Model |
| 07290117524008 - Tixel | 2021-11-01 Tixel Back Unit |
| 07290117524015 - Tixel Handpiece | 2021-11-01 Standard Handpiece used with TXLD0002 |
| 07290117524022 - Tixel Periorbital Handpiece | 2021-11-01Handpiece used with Tixel System TXLD0002 |
| 07290117524022 - Tixel Periorbital Handpiece | 2021-11-01 Handpiece used with Tixel System TXLD0002 |