Spatula 07-959-23

GUDID 04946329402551

Spatula 210 mm x 15 mm, Stainless

MIZUHO CORPORATION

Neurosurgical retraction system, brain

• Primary Device ID: 04946329402551
• NIH Device Record Key: 889e4f54-5405-4212-b067-187c71e900c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spatula
• Version Model Number: 07-959-23
• Catalog Number: 07-959-23
• 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: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp
• Phone: 9999999999
• Email: regulatory@mizuho.co.jp

Device Dimensions

• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter
• Length: 210 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04946329402551 [Primary]

FDA Product Code

• HAO: Instrument, Surgical, Non-Powered

Sterilization

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

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

[04946329402551]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-30
• Device Publish Date: 2023-05-22

On-Brand Devices [Spatula]

• 04946329389852: Spatula 2 mm Stainless
• 04946329389845: Spatula 4 mm Stainless
• 04946329389838: Spatula 6 mm Stainless
• 04946329402605: Spatula 140 mm x 20 mm, Stainless
• 04946329402599: Spatula 140 mm x 15 mm, Stainless
• 04946329402582: Spatula 140 mm x 10 mm, Stainless
• 04946329402575: Spatula 210 mm x 30 mm, Stainless
• 04946329402568: Spatula 210 mm x 20 mm, Stainless
• 04946329402551: Spatula 210 mm x 15 mm, Stainless
• 04946329402544: Spatula 210 mm x 10 mm, Stainless
• 04946329402537: Spatula 210 mm x 5 mm, Stainless