Primary Device ID | 00878953001791 |
NIH Device Record Key | 5324ef1b-c850-4743-aba8-c292f29fb671 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GreenLight HPS |
Version Model Number | 0010-0070H |
Company DUNS | 796308653 |
Company Name | AMERICAN MEDICAL SYSTEMS |
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 | 00878953001791 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-02-13 |
Device Publish Date | 2016-09-24 |
00878953001920 | Laser System |
00878953001807 | Laser System |
00878953001791 | Laser System |
00878953001784 | Laser System |
00878953000206 | Laser System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GREENLIGHT HPS 77030206 3421221 Live/Registered |
AMERICAN MEDICAL SYSTEMS, LLC 2006-10-26 |