| Primary Device ID | 00855357006041 |
| NIH Device Record Key | 75af2d7c-dfb4-4475-8e79-d388cd4fc994 |
| Commercial Distribution Discontinuation | 2018-10-24 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Rezūm Accessory Kit |
| Version Model Number | D2202 |
| Company DUNS | 947824194 |
| Company Name | NXTHERA, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 6123969849 |
| spetrie@libramed.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00855357006034 [Primary] |
| GS1 | 00855357006041 [Package] Contains: 00855357006034 Package: Box [5 Units] Discontinued: 2018-10-24 Not in Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2018-11-22 |
| Device Publish Date | 2017-07-17 |
| 08714729986843 - rezum Generator | 2019-11-19 |
| 08714729986850 - rezum Generator | 2019-11-19 |
| 08714729986867 - rezum Generator | 2019-11-19 |
| 08714729986874 - rezum Generator | 2019-11-19 |
| 00855357006003 - rezum Generator | 2019-11-19 |
| 00855357006010 - rezum | 2019-11-19 Delivery Device Kit for BPH |
| 00855357006041 - Rezūm Accessory Kit | 2018-11-22 |
| 00855357006041 - Rezūm Accessory Kit | 2018-11-22 |