AccessGUDID - DEVICE: ENDOLIGHT (04055207012895)

GUDID

Device Identifier (DI) Information

Brand Name: ENDOLIGHT
Version or Model: 5142001
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 5142001
Company Name: Richard Wolf GmbH

Primary DI Number: 04055207012895
Issuing Agency: GS1
Commercial Distribution End Date: March 01, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 315304071 *Terms of Use

Device Description: LIGHT SOURCE X 300 300W Xenon short arc lamp, LED, buttons, universal light cable connection, 6000K, U: 100-240VAC, 50/60Hz, Dim (wxhxd) 300x160x400mm

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?
35158	Endoscopic light source unit, line-powered	A mains electricity (AC-powered) unit designed to produce light of high intensity, often called cold light, for viewing surgical fields and body cavities during endoscopy (e.g., used with an arthroscope, cystoscope, laparoscope, gastroscope); it may have additional non-endoscopic lighting applications. It is designed as a bench-top unit with controls and a source of bright light [e.g., using a xenon (Xe) light bulb] that is channelled to the endoscope via a light cable to illuminate the site of observation/intervention while minimizing tissue heating.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GCT	Light source, endoscope, xenon arc

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: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 0e26903f-6327-4eb5-83c7-173fa0ec8dec
Public Version Date: May 24, 2023
Public Version Number: 7
DI Record Publish Date: July 21, 2017