Primary Device ID | 10653405008132 |
NIH Device Record Key | c8f85ce5-eae4-44ce-abf7-221a7f439931 |
Commercial Distribution Discontinuation | 2024-12-03 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 60-0136-002 |
Catalog Number | 60-0136-002 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10653405008132 [Primary] |
GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2024-12-04 |
Device Publish Date | 2016-09-24 |
10653405008125 - NA | 2024-12-04 CONMED REUSABLE DISPERSIVE ELECTRODE |
10653405008132 - NA | 2024-12-04CONMED REUSABLE PEDIATRIC DISPERSIVE ELECTRODE |
10653405008132 - NA | 2024-12-04 CONMED REUSABLE PEDIATRIC DISPERSIVE ELECTRODE |
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30653405987592 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz |
30653405987608 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit, 220V-240V 50/60 Hz |
30653405990141 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz |
20653405990120 - BioBrace | 2024-09-30 BioBrace® Reinforced Implant, 23 x 25 mm |
20653405990137 - BioBrace | 2024-09-30 BioBrace® Reinforced Implant, 35 x 25 mm |