AccessGUDID - DEVICE: NeuroTherm™ (05415067022363)

GUDID

Device Identifier (DI) Information

Brand Name: NeuroTherm™
Version or Model: RFDEUK-20
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: RFDEUK-20
Company Name: NEUROTHERM, INC.

Primary DI Number: 05415067022363
Issuing Agency: GS1
Commercial Distribution End Date: April 02, 2020
Device Count: 1
Labeler D-U-N-S® Number*: 124023552 *Terms of Use

Device Description: Disposable Radiofrequency 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:	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?
61931	Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use	A hand-held surgical instrument intended to be percutaneously introduced via a dedicated cannula [under external image guidance or using electrical stimulation for nerve location] to deliver radio-frequency current, in a monopolar configuration, from a system generator directly to peripheral nerve tissues to coagulate/ablate them for the treatment of pain. It includes a distal monopolar electrode which may include temperature-sensing elements; the introduction cannula or a tubing set to allow fluid cooling of the electrode may be included. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GXI	PROBE, RADIOFREQUENCY LESION

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: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Store in a cool dry place; avoid exposure to extreme temperatures.

Clinically Relevant Size

[?]

Size Type Text
Length: 20 Centimeter

Device Record Status

Public Device Record Key: 96168313-b78f-4ab3-b30b-14909f6ce1c7
Public Version Date: August 16, 2023
Public Version Number: 3
DI Record Publish Date: October 30, 2015