Endocavity Biopsy Starter Kit 10002814

GUDID 00841912106790

Stainless Steel Endocavity Biopsy Starter Kit for Alpinion EC2-11H & EV2-11H Ultrasound Transducers

PROTEK MEDICAL PRODUCTS, INC.

Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Nonimplantable needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable

• Primary Device ID: 00841912106790
• NIH Device Record Key: e3f6fdef-bea2-40ba-85c0-0ebdfb493b37
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endocavity Biopsy Starter Kit
• Version Model Number: 7182
• Catalog Number: 10002814
• Company DUNS: 965417181
• Company Name: PROTEK MEDICAL PRODUCTS, 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: true
• Device Combination Product: false
• Single Use: false
• 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	00841912106790 [Primary]

Sterilization

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

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

[00841912106790]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-15
• Device Publish Date: 2021-02-05

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• 00841912106790: Stainless Steel Endocavity Biopsy Starter Kit for Alpinion EC2-11H & EV2-11H Ultrasound Transduc