Biolox Delta Modular Head 32mm SHORT -4.0mm 12/14 104.3200

GUDID 05055196964341

BIOLOX Delta Ceramic Head

CORIN LTD

Ceramic femoral head prosthesis

• Primary Device ID: 05055196964341
• NIH Device Record Key: cf1d8e17-40da-4b33-9614-3d67bcd3cc8e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Biolox Delta Modular Head 32mm SHORT -4.0mm 12/14
• Version Model Number: 104.3200
• Catalog Number: 104.3200
• Company DUNS: 295437313
• Company Name: CORIN LTD
• 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

Customer Support Contacts

• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com
• Phone: +441285659866
• Email: lucinda.gerber@coringroup.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055196964341 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103120

FDA Product Code

• LZO: Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

Sterilization

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

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

[05055196964341]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-17

Devices Manufactured by CORIN LTD

• 05056139243271 - Unity Total Knee System: 2025-06-05 UNITY KNEE™ PS-C INSERT - Size 9 x 9mm
• 05056139243295 - Unity Total Knee System: 2025-06-05 UNITY KNEE™ PS-C INSERT - Size 9 x 10mm
• 05056139243325 - Unity Total Knee System: 2025-06-05 UNITY KNEE™ PS-C INSERT - Size 9 x 11mm
• 05056139243349 - Unity Total Knee System: 2025-06-05 UNITY KNEE™ PS-C INSERT - Size 9 x 12mm
• 05056139243363 - Unity Total Knee System: 2025-06-05 UNITY KNEE™ PS-C INSERT - Size 9 x 14mm
• 05056139243370 - Unity Total Knee System: 2025-06-05 UNITY KNEE™ PS-C INSERT - Size 1 x 16mm
• 05056139243387 - Unity Total Knee System: 2025-06-05 UNITY KNEE™ PS-C INSERT - Size 1 x 18mm
• 05056139243394 - Unity Total Knee System: 2025-06-05 UNITY KNEE™ PS-C INSERT - Size 9 x 16mm