Primary Device ID | 04250350109274 |
NIH Device Record Key | 66d06b68-1b56-4b1f-8da9-08bc29f152f1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Endovapor® |
Version Model Number | JEVN0001 |
Catalog Number | JEVN0001 |
Company DUNS | 344267187 |
Company Name | Joimax GmbH |
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 | 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 |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com | |
Phone | +497212551407010 |
info@joimax.com |
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 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 | 04250350109274 [Primary] |
GEI | Electrosurgical, cutting & coagulation & accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
[04250350109274]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-04-04 |
Device Publish Date | 2022-12-30 |
04250350109274 | joimax® Neutral Electrode |
04250337118848 | joimax® Endovapor®2 System |
04250337114604 | joimax® Endovapor®2 System |
04250337111832 | joimax® Endovapor®2 System |
04250337111825 | joimax® Endovapor®2 System |
04250337105626 | joimax® Neutral Electrode Connecting Cable |
04250337105381 | joimax® Endovapor® Surgi-Max® |
04250337103967 | joimax® Endovapor®2 Device |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ENDOVAPOR 79103148 4223743 Live/Registered |
Joimax GmbH 2011-08-08 |