AccessGUDID - DEVICE: SHARK/S-LINE (04055207000922)

GUDID

Device Identifier (DI) Information

Brand Name: SHARK/S-LINE
Version or Model: 8108252
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 8108.252
Company Name: Richard Wolf GmbH

Primary DI Number: 04055207000922
Issuing Agency: GS1
Commercial Distribution End Date: May 25, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 315304071 *Terms of Use

Device Description: HF BIPOLAR CONNECTING CABLE L 5M for ERBE generators, reusable

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:	No
Prescription Use (Rx):	No
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?
47487	Electrical-only medical device connection cable, reusable	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. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FAS	ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
Hydrogen Peroxide
Ethylene Oxide
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Length: 5 Meter

Device Record Status

Public Device Record Key: fc2e72e2-1dd5-4dd5-9812-4daadb75e86c
Public Version Date: November 21, 2024
Public Version Number: 6
DI Record Publish Date: September 26, 2016