Boneplate 10-5365

GUDID 04026575018444

Lanz and Kron

WALDEMAR LINK GmbH & Co. KG

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

• Primary Device ID: 04026575018444
• NIH Device Record Key: ba645123-1fc6-49a2-8f0f-c03f8eecd0f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Boneplate
• Version Model Number: 10-5365
• Catalog Number: 10-5365
• Company DUNS: 315675488
• Company Name: WALDEMAR LINK GmbH & Co. KG
• Device Count: 1
• DM Exempt: true
• 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: false
• Manufacturing Date: false
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	04026575018444 [Primary]

FDA Product Code

• HRS: Plate, Fixation, Bone

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-02-19
• Device Publish Date: 2015-11-01

On-Brand Devices [Boneplate]

• 04026575018499: Radial Plate
• 04026575018482: Radial Plate
• 04026575018475: Radial Plate
• 04026575018468: Radial Plate
• 04026575018451: Lanz and Kron
• 04026575018444: Lanz and Kron