Primary Device ID | 03700542625484 |
NIH Device Record Key | 9f4e38e9-129e-4e28-9a8d-6bdd1275ec32 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EASYRET |
Version Model Number | EASYRET |
Company DUNS | 738574953 |
Company Name | QUANTEL MEDICAL |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700542625484 [Primary] |
HQF | Laser, Ophthalmic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-04-21 |
Device Publish Date | 2017-09-11 |
03700542625484 | 577nm Fiber Technology Laser SingleSpot, MultiSpot and SubLiminal mode |
03700542625927 | The laser (577 nm Fiber Techology Laser SingleSpot, MultiSpot and Subliminal mode and Slit Lamp |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EASYRET 79196611 5215829 Live/Registered |
QUANTEL MEDICAL 2016-07-18 |