Primary Device ID | 00878953000152 |
NIH Device Record Key | 43fca015-245f-45b2-a0b3-f789835126cf |
Commercial Distribution Discontinuation | 2019-01-23 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | SureFlex |
Version Model Number | 8013060 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00878953000152 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-13 |
Device Publish Date | 2016-09-24 |
00878953004815 | 150 Lithotripsy Fiber |
00878953000190 | 910 µm Lithotripsy Fiber |
00878953000183 | 550 µm Lithotripsy Fiber |
00878953000169 | 365 µm Lithotripsy Fiber |
00878953000152 | 273 µm Lithotripsy Fiber |
00878953000145 | 200 µm Lithotripsy Fiber |
00878953000138 | 150 µm Lithotripsy Fiber |