RFTL Sono 001175-20A

GUDID 14048223024642

RFTL Sono 22G x 98,6mm, with Cornerstone reflectors

Pajunk GmbH Medizintechnologie

Radio-frequency ablation system probe cannula, single-use

• Primary Device ID: 14048223024642
• NIH Device Record Key: 6fb3c054-9648-4c5f-a788-a490020159a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RFTL Sono
• Version Model Number: 001175-20A
• Catalog Number: 001175-20A
• Company DUNS: 317654283
• Company Name: Pajunk GmbH Medizintechnologie
• Device Count: 25
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

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Device Identifiers

Device Issuing Agency	Device ID
GS1	04048223024645 [Unit of Use]
GS1	14048223024642 [Primary]

FDA Product Code

• GXI: PROBE, RADIOFREQUENCY LESION

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-01

On-Brand Devices [RFTL Sono]

• 14048223026080: RFTL Sono 22G x 98,6mm with Cornersto
• 14048223024642: RFTL Sono 22G x 98,6mm, with Cornersto
• 04048223026083: 001175-20B
• 04048223024645: 001175-20A
• 04048223050484: RFTL Sono 20G x 52,6 mm with Cornerstone reflectors