3312040

GUDID 30603295168618

DEPUY CMW 1 High Viscosity Bone Cement 40g

DEPUY (IRELAND)

Orthopaedic cement, non-medicated

• Primary Device ID: 30603295168618
• NIH Device Record Key: ad172806-aeab-4c9c-89a4-32e0924dafc3
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 3312-040
• Catalog Number: 3312040
• Company DUNS: 989365556
• Company Name: DEPUY (IRELAND)
• 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: 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

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	10603295168614 [Primary]
GS1	20603295168611 [Package]; Contains: 10603295168614; Package: PACKAGE [10 Units]; In Commercial Distribution
GS1	30603295168618 [Package]; Contains: 10603295168614; Package: CASE [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K053003

FDA Product Code

• LOD: BONE CEMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-07-19
• Device Publish Date: 2015-09-24

Devices Manufactured by DEPUY (IRELAND)

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• 10603295553915 - RECLAIM: 2025-08-04 RECLAIM MONOBLOC DISTAL REAMER SHORT 19