| Primary Device ID | 00817495023496 |
| NIH Device Record Key | 5ccb903f-c311-486f-a5ab-5c44b67805b0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vbeam Perfecta |
| Version Model Number | 9914-VT-0300 |
| Catalog Number | 9914-VT-0300 |
| Company DUNS | 053468385 |
| Company Name | CANDELA CORPORATION |
| 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 | 00817495023496 [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 | 2022-04-13 |
| Device Publish Date | 2022-04-05 |
| 00817495021478 | Pulsed Laser |
| 00817495021027 | Pulsed Laser |
| 00817495020600 | Pulsed Laser |
| 00817495020594 | Pulsed Laser |
| 00817495020266 | Pulsed Laser |
| 00817495020259 | Pulsed Laser |
| 00817495020136 | Pulsed Laser |
| 00817495020020 | Pulsed Laser |
| 00817495023496 | Pulse Dye Laser |
| 00817495020006 | Pulse Dye Laser |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VBEAM PERFECTA 85898271 4520330 Live/Registered |
Candela Corporation 2013-04-08 |