| Primary Device ID | 00817495023571 |
| NIH Device Record Key | bc665b2b-2368-4383-bc8a-b0ddcaa3381e |
| Commercial Distribution Discontinuation | 2024-10-14 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | GMAX Pro Plus Laser System |
| Version Model Number | 9914-CH-9036 |
| 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 |