Convenience Pack with 12" Flex Tube

GUDID 00816472020695

Convenience Pack with 12" Flex Tube

Intersurgical Incorporated

Anaesthesia breathing circuit, single-use

• Primary Device ID: 00816472020695
• NIH Device Record Key: f7231d62-cc0b-468c-ba9b-dd1be53a1d9d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Convenience Pack with 12" Flex Tube
• Version Model Number: B0028000
• Company DUNS: 785952607
• Company Name: Intersurgical Incorporated
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• 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

• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com
• Phone: 315-451-2900
• Email: support@intersurgicalinc.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816472020688 [Primary]
GS1	00816472020695 [Package]; Contains: 00816472020688; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• OFP: Anesthesia Breathing Circuit Kit (Adult & Pediatric)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-02-11
• Device Publish Date: 2023-01-25

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