Kitazato OPU Needle Type2-v6 351304

GUDID 14580303269142

KITAZATO CORPORATION

Soft-tissue biopsy procedure kit, non-medicated

• Primary Device ID: 14580303269142
• NIH Device Record Key: 920c1405-e032-48a8-bc9d-a63a8b289a17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kitazato OPU Needle Type2-v6
• Version Model Number: 351304 Type2-v6
• Catalog Number: 351304
• Company DUNS: 711091157
• Company Name: KITAZATO CORPORATION
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04580303269145 [Primary]
GS1	14580303269142 [Package]; Contains: 04580303269145; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112462

FDA Product Code

• MQE: NEEDLE, ASSISTED REPRODUCTION

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-08
• Device Publish Date: 2016-11-09

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• 14573316385978 - Ultra-Fast Vitri: 2025-09-05
• 14573316385985 - Ultra-Fast Vitri: 2025-09-05
• 14573316386012 - Ultra-Fast Vitri: 2025-09-05
• 14573316386029 - Ultra-Fast Vitri: 2025-09-05
• 14573316386173 - ES(Equilibration Solution) Pack 4 vials: 2024-12-03 ES(Equilibration Solution) Pack 4x1.5ml vials