Primary Device ID | 10845854040348 |
NIH Device Record Key | 7c59750d-753a-468c-a33d-02a3b49c4667 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LightWave |
Version Model Number | IA-2000-S |
Catalog Number | IA-2000-S |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
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 | false |
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 Issuing Agency | Device ID |
---|---|
GS1 | 10845854040348 [Primary] |
GS1 | 20845854040345 [Previous] |
GEI | Electrosurgical, cutting & coagulation & accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-18 |
Device Publish Date | 2024-04-10 |
20845854040369 | LIGHTWAVE ABLATOR 90 DEGREE ANGLE 3.2MM X 150MM |
20845854040352 | LIGHTWAVE ABLATOR, 90 DEGREE ANGLE, 3.2MM X 150MM |
20845854040345 | LIGHTWAVE SUCTION ABLATOR |
10845854040348 | LightWave Suction Ablator |