Advincula Arch Reusable Manipulator Handle

GUDID 00888937015225

Advincula Arch Reusable Manipulator Handle

Coopersurgical, Inc.

Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use Uterine manipulator, single-use

• Primary Device ID: 00888937015225
• NIH Device Record Key: 08845f16-682a-4436-be6a-f74bdb9267db
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Advincula Arch Reusable Manipulator Handle
• Version Model Number: UMH750
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	00888937015225 [Primary]

FDA Product Code

• LKF: Cannula, Manipulator/Injector, Uterine

Sterilization

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

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

[00888937015225]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-12-07
• Device Publish Date: 2022-11-29

Devices Manufactured by Coopersurgical, Inc.

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• 60888937027183 - ERPeak: 2024-04-18 IVD Sample kit
• 60888937027190 - ERPeak: 2024-04-18 IVD Sample kit
• 60888937027206 - ERPeak: 2024-04-18 IVD Sample kit
• 00888937026870 - Mara Console: 2024-03-21 Mara Console- Endometrial Ablation
• 00888937023817 - K-Systems: 2024-02-27 L126 IVF, Standard Heat Right
• 00888937023824 - K-Systems: 2024-02-27 L126 IVF, Standard Heat Right
• 00888937023831 - K-Systems: 2024-02-27 L126 IVF, RI Witness Right