IVF Pasteur Pipets

GUDID 50888937014056

Origio, Inc. 5.75" (14.6 cm) IVF Pasteur Pipets

Coopersurgical, Inc.

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• Primary Device ID: 50888937014056
• NIH Device Record Key: ec7bd1c9-e5e1-436d-b1cf-9117d1aa07f4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IVF Pasteur Pipets
• Version Model Number: PP-5.75-1000
• 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: 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	20888937014055 [Package]; Package: Box [20 Units]; In Commercial Distribution
GS1	50888937014056 [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: 3
• Public Version Date: 2020-03-30
• 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