| Primary Device ID | 07290109147338 |
| NIH Device Record Key | c53e6755-251a-4092-9104-42fe21498ce7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lumenis Pulse P120 30 Amp |
| Version Model Number | Lumenis Pulse P120 30 Amp |
| Catalog Number | GA-2009996D |
| Company DUNS | 600166524 |
| Company Name | LUMENIS 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 | 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 | 07290109147338 [Primary] |
| GEX | Powered Laser Surgical Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-27 |
| Device Publish Date | 2022-09-19 |
| 07290109147161 - Lumenis Pulse 120H | 2025-02-26 |
| 07290109147178 - Lumenis Pulse 120H | 2025-02-26 |
| 07290109147185 - Lumenis Pulse, Moses 2.0 (DOM) | 2025-02-26 |
| 07290109147192 - Lumenis Pulse 120H | 2025-02-26 |
| 07290109147208 - Lumenis Pulse, Moses 2.0 (INT) | 2025-02-26 |
| 07290109147215 - Lumenis Pulse 120H | 2025-02-26 |
| 07290109147222 - Lumenis Pulse 120H | 2025-02-26 |
| 07290109147291 - Lumenis Pulse 120H | 2025-02-26 |