Kitazato ET Catheter Type1-v6 EC-PRO Normal 205023

GUDID 14580303309510

4.7Fr 230mm EC-PRO Inner Catheter

KITAZATO CORPORATION

Assisted reproduction transfer catheter/set

• Primary Device ID: 14580303309510
• NIH Device Record Key: e20c9287-675e-4923-afc2-637d8c846912
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kitazato ET Catheter Type1-v6 EC-PRO Normal
• Version Model Number: 205023 Type1-v6 EC-PRO Normal
• Catalog Number: 205023
• 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	04580303309513 [Primary]
GS1	14580303309510 [Package]; Contains: 04580303309513; Package: [10 Units]; In Commercial Distribution

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: 2020-01-16
• Device Publish Date: 2020-01-08

On-Brand Devices [Kitazato ET Catheter Type1-v6 EC-PRO Normal]

• 04580303269510: 4.7Fr 230mm EC-PRO Inner Catheter
• 14580303309510: 4.7Fr 230mm EC-PRO Inner Catheter