Megasystem-C Tumor- and Revision System - Instruments

GUDID 04026575081967

Orthopaedic implant/instrument adaptor, reusable - General Instrument

WALDEMAR LINK GmbH & Co. KG

Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable

• Primary Device ID: 04026575081967
• NIH Device Record Key: 88ed5521-a7e0-4d79-8e96-024aae67e7a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Megasystem-C Tumor- and Revision System - Instruments
• Version Model Number: 16-3283/01
• Company DUNS: 315675488
• Company Name: WALDEMAR LINK GmbH & Co. KG
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04026575081967 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

[04026575081967]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-01-12
• Device Publish Date: 2023-01-04

On-Brand Devices [Megasystem-C Tumor- and Revision System - Instruments]

• 04026575081967: Orthopaedic implant/instrument adaptor, reusable - General Instrument
• 04026575242726: Orthopaedic implant aiming/guiding block, reusable - Megasystem-C Tumor- and Revision System
• 04026575242719: Orthopaedic implant aiming/guiding block, reusable - Megasystem-C Tumor- and Revision System
• 04026575242702: Orthopaedic implant aiming/guiding block, reusable - Megasystem-C Tumor- and Revision System