ET CATHETER RYDEN 223352

GUDID 14580745044239

KITAZATO CORPORATION

Assisted reproduction transfer catheter/set

• Primary Device ID: 14580745044239
• NIH Device Record Key: 117b09b5-530a-4b02-8a46-8865ce26f1ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ET CATHETER RYDEN
• Version Model Number: ET-C3022PMOS+G17ASRT
• Catalog Number: 223352
• 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: false
• Manufacturing Date: true
• 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	14580745044239 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162878

FDA Product Code

• MQF: Catheter, Assisted Reproduction

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-25
• Device Publish Date: 2025-09-17

On-Brand Devices [ET CATHETER RYDEN]

• 14580745044246: ET-C3025PMOS+G20ASRT
• 14580745044239: ET-C3022PMOS+G17ASRT
• 14580745043904: ET-C3022PMOS-G17ASRT
• 14580745043782: ET-C3025PMOS-G20ASRT