DEVICE: CONMED (30653405011266)
Device Identifier (DI) Information
CONMED
60-5806-001
Not in Commercial Distribution
60-5806-001
Conmed Corporation
60-5806-001
Not in Commercial Distribution
60-5806-001
Conmed Corporation
REUSABLE GROUNDING PAD CABLES
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| No | |
| Yes | |
| No | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 63401 | Electrosurgical return lead |
An insulated metal wire(s) intended to connect an electrosurgical return electrode (not included) to an electrosurgical/radio-frequency ablation system generator, to allow return of electrical current from the patient to the generator during monopolar electrosurgery. This is a reusable device.
|
Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| K771007 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Handling Environment Humidity: between 30 and 75 Percent (%) Relative Humidity |
| Handling Environment Temperature: between 16 and 27 Degrees Celsius |
| Handling Environment Temperature: between -29 and 50 Degrees Celsius |
| Storage Environment Temperature: between 10 and 32 Degrees Celsius |
| Handling Environment Temperature: between 60 and 80 Degrees Fahrenheit |
| Storage Environment Humidity: between 10 and 90 Percent (%) Relative Humidity |
| Handling Environment Temperature: between -20 and 120 Degrees Fahrenheit |
| Handling Environment Humidity: less than 85 Percent (%) Relative Humidity |
| Storage Environment Temperature: between 50 and 90 Degrees Fahrenheit |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| No Device Sizes |
Device Record Status
bba23896-f06e-46f4-b320-144c9d9d506b
November 18, 2024
6
September 24, 2016
November 18, 2024
6
September 24, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(866)426-6633
CustomerExperience@conmed.com
CustomerExperience@conmed.com