Primary Device ID | 08033945934712 |
NIH Device Record Key | 014660f9-7f98-4fbe-9b0e-69203cbd783d |
Commercial Distribution Discontinuation | 2018-11-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Quantaforte |
Version Model Number | OAM001909 |
Company DUNS | 436045833 |
Company Name | QUANTA SYSTEM SPA |
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 | 08033945934712 [Primary] |
ONF | Powered Light Based Non-Laser Surgical Instrument With Thermal Effect |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-07-01 |
Device Publish Date | 2016-08-29 |
08033945934743 | Laser diode handpiece 808 nm |
08033945934729 | Nd:YAG laser handpiece 1064 nm |
08033945934712 | Intense pulsed light handpiece 635-950 nm |
08033945934705 | Intense Pulsed Light handpiece 580-950 nm SR |
08033945934699 | Intense Pulsed Light handpiece 580-950 nm HR |
08033945934682 | Intense Pulsed Light handpiece 535-950 nm |
08033945934675 | Intense Pulsed Light handpiece 415-950 nm |
08033945934736 | 2940 nm Erbium:YAg handpiece |