AccessGUDID - DEVICE: NA (04055207063392)

GUDID

Device Identifier (DI) Information

Brand Name: NA
Version or Model: 2260003
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 2260003
Company Name: Richard Wolf GmbH

Primary DI Number: 04055207063392
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 315304071 *Terms of Use

Device Description: HF SURGERY GENERATOR 400KHZ for Urology, Gynecology, Surgery, for the connection of monopolar and bipolar accessories, international version for USA, monopolar connection Bovie, 3-pin, 4mm plug, bipolar connection, Erbe, Valleylab, touch screen, color display, compatible with core nova, connection socket for neutral electrode cable international, U: 100-240VAC, 50/60Hz, Dim. (wxhxd) 300x159x416

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?
11490	Electrosurgical system generator	An electrically-powered component of a electrosurgical system intended to generate radio-frequency (RF) electrical current for subsequent cutting and coagulation of soft tissues during an endoscopic or open surgical procedure; it is not dedicated to focal ablation of specific tissues (i.e., not a radio-frequency ablation system generator). It includes controls, may include an integrated surgical plume (smoke) suction unit, and is intended to be connected via a cable to an electrosurgical handpiece and electrode (neither of these are included); it is not intended for inert gas-enhanced electrosurgery.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEI	Electrosurgical, cutting & coagulation & accessories

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K230194	000

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
Storage Environment Humidity: between 10 and 90 Percent (%) Relative Humidity
Storage Environment Temperature: between -20 and 60 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 5d4af909-01c1-4317-9480-787797e7e3d8
Public Version Date: November 21, 2024
Public Version Number: 3
DI Record Publish Date: July 07, 2023