Spetzler® Micro Dissection Set, Tray #3

GUDID 00840096215151

Spetzler® Micro Dissection Set, Tray #3

KATALYST SURGICAL LLC

Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable

• Primary Device ID: 00840096215151
• NIH Device Record Key: 70b9c207-ca7a-4015-8668-d9fee52a2256
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spetzler® Micro Dissection Set, Tray #3
• Version Model Number: N4409-SET
• Company DUNS: 007883297
• Company Name: KATALYST SURGICAL LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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	00840096215151 [Primary]

Sterilization

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

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

[00840096215151]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-15
• Device Publish Date: 2023-12-07

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