Primary Device ID | 08809578390016 |
NIH Device Record Key | e9e7c5bd-812e-4160-a140-a6a7f17f0f95 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Q-Switched Nd:YAG Laser |
Version Model Number | Q10 |
Company DUNS | 689046045 |
Company Name | IDS Ltd |
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 | false |
OTC Over-The-Counter | false |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr | |
Phone | +82220251153 |
info@ids.co.kr |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809578390016 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-11 |
Device Publish Date | 2019-06-03 |
08809578390313 - Picosecond Nd:YAG Laser | 2024-01-05 |
08809578390344 - Alexandrite & Long Pulsed Nd:YAG Laser | 2023-04-17 |
08809578390030 - Phototherapy Unit | 2021-10-19 |
08809578390016 - Q-Switched Nd:YAG Laser | 2019-06-11 |
08809578390016 - Q-Switched Nd:YAG Laser | 2019-06-11 |