Vbeam Perfecta
GUDID 00817495020006
Pulse Dye Laser
CANDELA CORPORATION
Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system Dermatological dye laser system| Primary Device ID | 00817495020006 |
| NIH Device Record Key | 7bd9e31f-ac5d-41b6-ae50-6dc9f5f228e6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vbeam Perfecta |
| Version Model Number | 9914-08-0300 |
| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817495020006 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
FDA Product Code
| GEX | Powered Laser Surgical Instrument |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-04-18 |
| Device Publish Date | 2022-04-08 |
On-Brand Devices [Vbeam Perfecta]
| 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 |
Trademark Results [Vbeam Perfecta]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VBEAM PERFECTA 85898271 4520330 Live/Registered |
Candela Corporation 2013-04-08 |
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