Primary Device ID | M47320444SMA0 |
NIH Device Record Key | 3b34fc86-fc8a-46ae-8061-336fc5ac8b3c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trimedyne® VaporMax® - Ho:YAG Side Firing Fiber-Optic Instrument |
Version Model Number | 20444-SMA |
Catalog Number | 20444-SMA |
Company DUNS | 057007239 |
Company Name | TRIMEDYNE, INC. |
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 |
---|---|
HIBCC | M47320444SMA0 [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 | 2 |
Public Version Date | 2020-02-27 |
Device Publish Date | 2018-07-11 |
M47320444SMA0 | VaporMax Sidefiring Fiber, SMA Connector |
M473204440 | VaporMax Sidefiring Fiber, TMED Connector |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRIMEDYNE 74055774 1636817 Live/Registered |
Trimedyne, Inc. 1990-05-04 |