Saturn 5 Laser System 6-47-500-26

GUDID 05060488044823

Assisted Reproduction Laser

RESEARCH INSTRUMENTS LIMITED

Assisted reproduction laser system

• Primary Device ID: 05060488044823
• NIH Device Record Key: 4df46f7d-1714-475b-bc9c-da6d1c329a7d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Saturn 5 Laser System
• Version Model Number: Saturn 5 Active 40x Nikon Ti2 with Nikon XY Stage
• Catalog Number: 6-47-500-26
• Company DUNS: 536139413
• Company Name: RESEARCH INSTRUMENTS LIMITED
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com
• Phone: +4546790202
• Email: origio@origio.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060488044823 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141434

FDA Product Code

• MRX: System, assisted reproduction laser

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2018-02-23

On-Brand Devices [Saturn 5 Laser System]

• 05060488044915: Assisted Reproduction Laser
• 05060488044847: Assisted Reproduction Laser
• 05060488044830: Assisted Reproduction Laser
• 05060488044823: Assisted Reproduction Laser
• 05060488044816: Assisted Reproduction Laser
• 05060488043789: Assisted Reproduction Laser
• 05060488043772: Assisted Reproduction Laser
• 05060488043635: Assisted Reproduction Laser
• 05060488043628: Assisted Reproduction Laser
• 05060488043406: Assisted Reproduction Laser
• 05060488043338: Assisted Reproduction Laser
• 05060488043277: Assisted Reproduction Laser
• 05060488042812: Assisted Reproduction Laser
• 05060488042768: Assisted Reproduction Laser
• 05060488042751: Assisted Reproduction Laser
• 05060488042744: Assisted Reproduction Laser
• 05060488042737: Assisted Reproduction Laser
• 05060488042720: Assisted Reproduction Laser
• 05060488042713: Assisted Reproduction Laser
• 05060488042706: Assisted Reproduction Laser
• 05060488042690: Assisted Reproduction Laser
• 05060488042683: Assisted Reproduction Laser
• 05060488042676: Assisted Reproduction Laser
• 05060488042669: Assisted Reproduction Laser
• 05060488042409: Assisted Reproduction Laser
• 05060488042393: Assisted Reproduction Laser
• 05060488041747: Assisted Reproduction Laser
• 05060488041730: Assisted Reproduction Laser
• 05060488041723: Assisted Reproduction Laser
• 05060488041716: Assisted Reproduction Laser
• 05060488041709: Assisted Reproduction Laser
• 05060488041693: Assisted Reproduction Laser
• 05060170183793: Assisted Reproduction Laser
• 05060170183786: Assisted Reproduction Laser