Endosee Advance Cannula with Pipet

GUDID 20888937022005

Endosee Advance Cannula with Pipet - 1 Kit - Contains - 1 Cannula and 1 Pipet Curet Endometrial Suction Curette 3mm OD

Coopersurgical, Inc.

Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use Intrauterine cannula, single-use

• Primary Device ID: 20888937022005
• NIH Device Record Key: 515be586-0eeb-4632-8f2e-7ba32c1cbfb6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endosee Advance Cannula with Pipet
• Version Model Number: ESPX5
• 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: false
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	20888937022005 [Package]; Contains: 60888937022003; Package: Box [5 Units]; In Commercial Distribution
GS1	60888937022003 [Primary]

FDA Product Code

• FAJ: Cystoscope And Accessories, Flexible/Rigid

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: 2023-05-17
• Device Publish Date: 2019-05-16

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