KONG-TL VBR System, KONG-TL VBR E, Container, complete 44-090

GUDID 07640172551523

KONG-TL VBR System, KONG-TL VBR E, Container, complete

icotec AG

Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable

• Primary Device ID: 07640172551523
• NIH Device Record Key: 5de702e5-bd0b-491e-84ea-d44313199837
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KONG-TL VBR System, KONG-TL VBR E, Container, complete
• Version Model Number: 44-090
• Catalog Number: 44-090
• Company DUNS: 480789465
• Company Name: icotec AG
• 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: true
• Serial Number: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch
• Phone: +41717570000
• Email: info@icotec.ch

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640172551523 [Primary]

FDA Product Code

• MQP: Spinal Vertebral Body Replacement Device

Sterilization

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

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

[07640172551523]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-18
• Device Publish Date: 2023-09-08

On-Brand Devices [KONG-TL VBR System, KONG-TL VBR E, Container, complete]

• 07640172551523: KONG-TL VBR System, KONG-TL VBR E, Container, complete
• 07640164847870: KONG-TL VBR System, KONG-TL VBR E, Container, complete