AccessGUDID - DEVICE: CONMED (10653405001881)

GUDID

Device Identifier (DI) Information

Brand Name: CONMED
Version or Model: 60-5102-002
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 60-5102-002
Company Name: Conmed Corporation

Primary DI Number: 10653405001881
Issuing Agency: GS1
Commercial Distribution End Date: January 25, 2023
Device Count: 10
Labeler D-U-N-S® Number*: 071595540 *Terms of Use

Device Description: CONMED DISPOSABLE BIPOLAR CABLE, 10' (3.05M)

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
47143	Electrical-only medical device connection cable, single-use	A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. Some types may include an electrical isolator to prevent electrical shocks, and/or a cable cover. This is a single-use 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 [?]
K893732	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Length: 3.05 Meter
Length: 10 Feet

Device Record Status

Public Device Record Key: adc7db37-24b5-4d40-8aec-32b4c1e322a0
Public Version Date: January 26, 2023
Public Version Number: 5
DI Record Publish Date: September 24, 2016