FISH 7 Fr CombiClose Vascular Closure Device

GUDID 00858241005021

MORRIS INNOVATIVE, INC.

Femoral artery catheter introduction/wound closure set

• Primary Device ID: 00858241005021
• NIH Device Record Key: c59f5768-f9f9-4b59-8f74-95d902b0b45d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FISH 7 Fr CombiClose Vascular Closure Device
• Version Model Number: 16-07-01-S
• Company DUNS: 005036225
• Company Name: MORRIS INNOVATIVE, INC.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00858241005021 [Primary]

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-08-17
• Device Publish Date: 2014-09-16

Devices Manufactured by MORRIS INNOVATIVE, INC.

• 00858241005007 - FISH 5 Fr CombiClose Vascular Closure Device: 2018-08-17
• 00858241005014 - FISH 6 Fr CombiClose Vascular Closure Device: 2018-08-17
• 00858241005021 - FISH 7 Fr CombiClose Vascular Closure Device: 2018-08-17
• 00858241005021 - FISH 7 Fr CombiClose Vascular Closure Device: 2018-08-17
• 00858241005038 - FISH 8 Fr CombiClose Vascular Closure Device: 2018-08-17
• 00858241005045 - FISH 6 Fr ControlClose Vascular Closure Device: 2018-08-17
• 00858241005052 - FISH 7 Fr ControlClose Vascular Closure Device: 2018-08-17