Ruskin Liston Bone Cutter 19cm Cvd 12-066-19

GUDID G25012066190

A strongly constructed, hand-held, surgical instrument designed to separate a bone into two parts through a cutting action. It typically consists of an instrument having one or two sharp robust blades that close over the bone and cut it. It is available in various designs: 1) a pliers-like design with elongated blades, or 2) twin angled blades attached to strong, sprung (self-opening), pivoted or multi-pivoted handles; that, when squeezed together, close the blades so that they cut entirely through the bone. Also known as bone shears, it is mainly used in orthopaedic surgical procedures and oral surgery. This is a reusable device.

N S SURGICAL COMPANY

Bone cutter

• Primary Device ID: G25012066190
• NIH Device Record Key: 15c8e33d-654a-4731-9d6b-33ae30b09d0f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ruskin Liston Bone Cutter 19cm Cvd
• Version Model Number: 12-066-19
• Catalog Number: 12-066-19
• Company DUNS: 645681649
• Company Name: N S SURGICAL COMPANY
• 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: false
• 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: false
• OTC Over-The-Counter: false

Device Dimensions

• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G25012066190 [Primary]

FDA Product Code

• FZT: Cutter, Surgical

Sterilization

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

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

[G25012066190]

Ethylene Oxide;Ultraviolet Light;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-05
• Device Publish Date: 2023-03-28

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