CONTOUR-Ribbed 2 - Instruments

GUDID 04026575415656

Orthopaedic prosthesis instrument, reusable - General Instrument

WALDEMAR LINK GmbH & Co. KG

Orthopaedic implant impactor, reusable

• Primary Device ID: 04026575415656
• NIH Device Record Key: 70d0615f-1a21-4439-99da-df3cdc92f5b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONTOUR-Ribbed 2 - Instruments
• Version Model Number: 130-600/03
• 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	04026575415656 [Primary]

FDA Product Code

• HWR: DRIVER, PROSTHESIS

Sterilization

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

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

[04026575415656]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2026-02-09
• Device Publish Date: 2022-12-19

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