Cuff:Inflation for ROSI 200812

GUDID 00817122020430

Part Number 200812, Cuff: Inflation for ROSI

VASCULAR TECHNOLOGY, INCORPORATED

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• Primary Device ID: 00817122020430
• NIH Device Record Key: 41fd5599-68ac-4cae-9998-120c52ef7c4f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cuff:Inflation for ROSI
• Version Model Number: 200812
• Catalog Number: 200812
• Company DUNS: 161989343
• Company Name: VASCULAR TECHNOLOGY, INCORPORATED
• Device Count: 1
• DM Exempt: true
• 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: 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: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com
• Phone: +1(603)594-9700
• Email: info@vti-online.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817122020430 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141323

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

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: 2018-07-06
• Device Publish Date: 2016-09-20

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