AccessGUDID - DEVICE: REUSABLE STRAIGHT NEEDLE ELECTRODE (00192896009264)

GUDID

Device Identifier (DI) Information

Brand Name: REUSABLE STRAIGHT NEEDLE ELECTRODE
Version or Model: A833
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: A833
Company Name: SONTEC INSTRUMENTS, INC.

Primary DI Number: 00192896009264
Issuing Agency: GS1
Commercial Distribution End Date: October 16, 2020
Device Count: 1
Labeler D-U-N-S® Number*: 040729840 *Terms of Use

Device Description: REUSABLE STRAIGHT NEEDLE ELECTRODE

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):	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?
32684	Endoscopic electrosurgical handpiece/electrode, bipolar, reusable	An electrosurgical device which consists of a handpiece with mechanical and/or electrical controls, and a bipolar electrode intended to deliver electrosurgical current from a system generator directly to tissues for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery; it may in addition be intended for open surgery. It includes a long thin electrode connected to the handpiece, and may include a lumen for suction/irrigation; it is available in a variety of forms (e.g., forceps, rigid probe with controls). 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 [?]
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 [?]
Moist Heat or Steam Sterilization
Dry Heat Sterilization

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: 7ac4e483-3013-4ea2-975b-c6b30c8e1c3c
Public Version Date: October 19, 2020
Public Version Number: 2
DI Record Publish Date: August 16, 2018