STOCKERT EP/IO Interface Box https://gudid.fda.gov/gudid/app/admin/udi/recordDe

GUDID 04260166370621

Stockert GmbH

Radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator Percutaneous radio-frequency ablation system generator

• Primary Device ID: 04260166370621
• NIH Device Record Key: c02d7a99-2cab-4bd6-b153-d9f4ed444af1
• Commercial Distribution Discontinuation: 2015-12-08
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: STOCKERT EP/IO Interface Box
• Version Model Number: S7032
• Catalog Number: https://gudid.fda.gov/gudid/app/admin/udi/recordDe
• Company DUNS: 327536314
• Company Name: Stockert GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260166370621 [Primary]

FDA Product Code

• DRF: Catheter, Electrode Recording, Or Probe, Electrode Recording

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-05-10
• Device Publish Date: 2014-09-23

On-Brand Devices [STOCKERT EP/IO Interface Box]

• 04260166370621: S7032
• 04260166370300: S7030