GLENOID REAMER WITH CANNULATED PIN 9C13.75.165

GUDID 08033390105729

GLENOID REAMER STD WITH CANNULATED PIN

LIMACORPORATE SPA

Bone-resection orthopaedic reamer, reusable

• Primary Device ID: 08033390105729
• NIH Device Record Key: 0f7094cf-5edf-4c07-b3b9-01c0b542c96e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GLENOID REAMER WITH CANNULATED PIN
• Version Model Number: GLENOID REAMER
• Catalog Number: 9C13.75.165
• Company DUNS: 432066322
• Company Name: LIMACORPORATE SPA
• 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: true
• Serial Number: false
• Manufacturing Date: false
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033390105729 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100858

FDA Product Code

• KWT: Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented

Sterilization

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

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

[08033390105729]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-07-23
• Device Publish Date: 2016-08-05

On-Brand Devices [GLENOID REAMER WITH CANNULATED PIN]

• 08033390105736: GLENOID REAMER LARGE WITH CANNULATED PIN
• 08033390105729: GLENOID REAMER STD WITH CANNULATED PIN
• 08033390105712: GLENOID REAMER SMALL R WITH CANNULATED PIN