CLEARCUT 415-00-120

GUDID 03760177046603

TEKNIMED

Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable Polymer orthopaedic cement restrictor, bioabsorbable

• Primary Device ID: 03760177046603
• NIH Device Record Key: a88f28fe-ba00-41c9-a168-ac857e3f3dd7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLEARCUT
• Version Model Number: Diameter 12
• Catalog Number: 415-00-120
• Company DUNS: 764746723
• Company Name: TEKNIMED
• 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: true
• Lot Batch: true
• Serial Number: true
• 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 Dimensions

• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter
• Outer Diameter: 12 Millimeter

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760177046603 [Primary]

FDA Product Code

• LZN: Cement Obturator

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-03
• Device Publish Date: 2020-11-25

On-Brand Devices [CLEARCUT]

• 03760177046535: Diameter 06
• 03760177046696: Diameter 18
• 03760177046665: Diameter 16
• 03760177046634: Diameter 14
• 03760177046603: Diameter 12
• 03760177046573: Diameter 10
• 03760177046542: Diameter 08