Zilver Flex ZFV6-35-125-10-40

GUDID 10827002183183

Zilver Flex 35 Vascular Stent

COOK IRELAND LTD

Peripheral artery stent, bare-metal

• Primary Device ID: 10827002183183
• NIH Device Record Key: 0fcee867-c6cd-44be-96fa-a471d98c012c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zilver Flex
• Version Model Number: G18318
• Catalog Number: ZFV6-35-125-10-40
• Company DUNS: 988559035
• Company Name: COOK IRELAND LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com
• Phone: +1(812)330-5494
• Email: sharedservices@cookmedical.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.
• Special Storage Condition, Specify: Between 0 and 0 *Store the device in a dry location.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00827002183186 [Primary]
GS1	10827002183183 [Package]; Contains: 00827002183186; Package: BX [1 Units]; In Commercial Distribution

FDA Product Code

• NIP: STENT, SUPERFICIAL FEMORAL ARTERY

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-12
• Device Publish Date: 2025-12-04

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