Sugita Titanium Clip II Single Shaft Applier 17-013-71

GUDID 04946329276435

Sugita Titanium Clip II Single Shaft Applier Mini, 50mm

MIZUHO CORPORATION

Aneurysm clip applier

• Primary Device ID: 04946329276435
• NIH Device Record Key: 17d44202-0ad1-4bc3-b885-366af8a0f9df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sugita Titanium Clip II Single Shaft Applier
• Version Model Number: 17-013-71
• Catalog Number: 17-013-71
• Company DUNS: 690677802
• Company Name: MIZUHO CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Serial Number: false
• 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: 800 699 2547
• Email: mizuho@mizuho.com

Device Dimensions

• Length: 204 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04946329276435 [Primary]

FDA Product Code

• HCI: Applier, Aneurysm Clip

Sterilization

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

[04946329276435]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-06-24

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