Kitazato OPU Needle with Connection Tube, Type2-v13 329001

GUDID 14580303269838

19G350mm, L Stopper

KITAZATO CORPORATION

Soft-tissue biopsy procedure kit, non-medicated

• Primary Device ID: 14580303269838
• NIH Device Record Key: 9bbc03fc-b719-4e96-9400-cf3d1067eae6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kitazato OPU Needle with Connection Tube, Type2-v13
• Version Model Number: 329001 Type2-v13
• Catalog Number: 329001
• 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	04580303269831 [Primary]
GS1	14580303269838 [Package]; Contains: 04580303269831; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162881

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: 2
• Public Version Date: 2020-01-08
• Device Publish Date: 2019-06-01

On-Brand Devices [Kitazato OPU Needle with Connection Tube, Type2-v13]

• 14580303269401: 359354 Type2-v13
• 14580303269838: 19G350mm, L Stopper