| Primary Device ID | 00817371020618 |
| NIH Device Record Key | a694635f-d2ec-4270-aa50-5c90ace17939 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ThermiRF+ |
| Version Model Number | ThermiRF+ |
| Company DUNS | 021008486 |
| Company Name | Thermi |
| 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 | false |
| 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 | 00817371020618 [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 | 2022-09-13 |
| Device Publish Date | 2022-09-05 |
| 00817371020618 - ThermiRF+ | 2022-09-13Thermi radio frequency generator |
| 00817371020618 - ThermiRF+ | 2022-09-13 Thermi radio frequency generator |
| 00817371020359 - ARVATI | 2021-09-30 Temperature Control Radiofrequency Generator |
| 00817371020014 - ThermiRF | 2019-08-09 Thermi Radio Frequency Generator |
| 00817371020021 - ThermiSmooth | 2019-08-09 ThermiSmooth Radiofrequency Generator |
| 00817371020038 - ThermiVA | 2019-08-09 ThermiVa Radiofrequency Generator |
| 00817371020045 - ThermiEyes | 2019-08-09 ThermiEyes Radiofrequency Generator |
| 00817371020113 - Thermi Classic Radiofrequency Cannula | 2019-02-07 Radiofrequency Cannula - Straight Blunt |
| 00817371020212 - Injectable RF Electrode | 2019-02-07 Disposable Radiofrequency Cannula Electrode |