TITAN WTIVFE-W5240

GUDID 00888937020328

In Vitro Fertilization IVF Workstation

RESEARCH INSTRUMENTS LIMITED

Class-I biological safety cabinet

• Primary Device ID: 00888937020328
• NIH Device Record Key: 07a16f6d-6364-4fc1-9230-93976a044007
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TITAN
• Version Model Number: TITAN WTIVFE IVF 240V SERIAL NUMBER
• Catalog Number: WTIVFE-W5240
• Company DUNS: 536139413
• Company Name: RESEARCH INSTRUMENTS LIMITED
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888937020328 [Primary]

FDA Product Code

• PUB: Accessory, Assisted Reproduction, Exempt

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-09-30
• Device Publish Date: 2024-09-20

On-Brand Devices [TITAN]

• 00888937024722: In Vitro Fertilization IVF Workstation
• 00888937020335: In Vitro Fertilization IVF Workstation
• 00888937020328: In Vitro Fertilization IVF Workstation
• 00888937014679: In Vitro Fertilization IVF Workstation
• 00888937014662: In Vitro Fertilization IVF Workstation
• 00888937014655: In Vitro Fertilization IVF Workstation
• 00888937014488: In Vitro Fertilization IVF Workstation