| Primary Device ID | 00817495022192 |
| NIH Device Record Key | 33793697-017f-4c39-9eea-aa67c0165e8a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Alex TriVantage 532/1064 Handpiece Assembly |
| Version Model Number | 7122-00-1207 |
| 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 | 00817495022192 [Primary] |
| GS1 | 08174950202196 [Previous] |
| GEX | Powered Laser Surgical Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-06-17 |
| Device Publish Date | 2016-09-23 |
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| 00817495025087 - Refurbished Applicator Frax 1940 | 2025-05-28 Refurbished Applicator Frax 1940 |
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| 00817495023526 - 1940 Applicator | 2025-03-14 1940 applicator (1940 nm) for Nordlys and Nordlys Mini |
| 00817495023953 - 1550 Applicator | 2025-03-14 1550 Applicator (1550 nm) for Nordlys and Nordlys Mini |
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| 00817495025247 - Vbeam Prima Pro DCD Handpiece | 2025-01-23 ASSY, DCD HP, DELIVERY SYSTEM, VBEAM PRIMA PRO |
| 00817495024677 - PicoWay Laser System | 2024-10-21 PicoWay Laser System |