AccessGUDID - DEVICE: SPINERY Connections (00860011603627)

GUDID

Device Identifier (DI) Information

Brand Name: SPINERY Connections
Version or Model: SP-CD
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: AXON SRL

Primary DI Number: 00860011603627
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 439154305 *Terms of Use

Device Description: SpineryTM Connections are cooling tubing to connect the needle handle with the cooling solution.The connection provides send and return of sterile saline water from the bag to connected needle. The double connection cooling tube is for use with two bipolar RF needles with a product code of SP-CD.

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?
66753	Percutaneous radio-frequency ablation probe cooling tubing set	A collection of flexible tubing and associated items that may include clamps, filters, and connectors, intended to be used with a peristaltic pump to deliver closed-loop circulation of a cooling solution (e.g., saline, sterile water) to a percutaneous radio-frequency ablation probe at a specified flow rate during a percutaneous ablation procedure. The tubing is made of synthetic material and is of a fixed diameter that is specific to the requirements of the pump. This is a single-use 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 [?]
K223303	000

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: b0e37ee6-57ef-4702-aa41-0a0496b605aa
Public Version Date: June 10, 2024
Public Version Number: 1
DI Record Publish Date: May 31, 2024