Duesseldorf Type Bell Partial Titanium 1002032

GUDID EHKM10020321

Ossicular Prosthesis, partial

Heinz Kurz GmbH

Ossicular prosthesis, partial

• Primary Device ID: EHKM10020321
• NIH Device Record Key: 5fec08ba-da8a-48c7-ae38-1508e1e6d409
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Duesseldorf Type Bell Partial Titanium
• Version Model Number: 1002032
• Catalog Number: 1002032
• Company DUNS: 341155720
• Company Name: Heinz Kurz GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: +49707291790
• Email: info@kurzmed.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EHKM10020321 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K972492

FDA Product Code

• ETB: Prosthesis, Partial Ossicular Replacement

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: 2018-07-06
• Device Publish Date: 2015-09-21

On-Brand Devices [Duesseldorf Type Bell Partial Titanium]

• EHKM10020331: Ossicular Prosthesis, partial
• EHKM10020321: Ossicular Prosthesis, partial
• EHKM10020301: Ossicular Prosthesis, partial
• EHKM10020291: Ossicular Prosthesis, partial
• EHKM10020281: Ossicular Prosthesis, partial
• EHKM10020271: Ossicular Prosthesis, partial
• EHKM10020261: Ossicular Prosthesis, partial