HydroFrame Framing Coil 101243HFRM-V

GUDID 00810170017230

V-Trak

MICROVENTION INC.

Neurovascular embolization coil

• Primary Device ID: 00810170017230
• NIH Device Record Key: 606e7e9a-2a95-42ba-88ae-ea789e29a508
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HydroFrame Framing Coil
• Version Model Number: 101243HFRM-V-A
• Catalog Number: 101243HFRM-V
• Company DUNS: 003263105
• Company Name: MICROVENTION INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(714)247-8000
• Email: customerservice@microvention.c
• Phone: +1(714)247-8000
• Email: customerservice@microvention.c

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810170017230 [Primary]

FDA Product Code

• KRD: Device, Vascular, for Promoting Embolization

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: 2018-09-07
• Device Publish Date: 2018-08-07

On-Brand Devices [HydroFrame Framing Coil]

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