IVF Pasteur Pipets

GUDID 20888937014093

Origio, Inc. 9" (22.9 cm) IVF Pasteur Pipets

Coopersurgical, Inc.

User-induced pipette

• Primary Device ID: 20888937014093
• NIH Device Record Key: 0ee5836e-77e2-4ca8-9289-aa04caa24d47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IVF Pasteur Pipets
• Version Model Number: PP-9-1000
• Company DUNS: 801895244
• Company Name: Coopersurgical, Inc.
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	20888937014093 [Package]; Contains: 50888937014094; Package: [20 Units]; In Commercial Distribution
GS1	50888937014094 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K000915

FDA Product Code

• MQK: Labware, 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: 2018-03-29
• Device Publish Date: 2016-09-23

On-Brand Devices [IVF Pasteur Pipets]

• 20888937014116: Origio, Inc. 9" (22.9 cm) IVF Pasteur Pipets
• 20888937014093: Origio, Inc. 9" (22.9 cm) IVF Pasteur Pipets
• 20888937014079: Origio, Inc. 5.75" (14.6 cm) IVF Pasteur Pipets
• 50888937014056: Origio, Inc. 5.75" (14.6 cm) IVF Pasteur Pipets