Biolox® Option NJ437T

GUDID 04038653462650

SLEEVE 8/10 L F/BIOLOX REVISION HEAD

Aesculap AG

Femoral head/stem prosthesis adaptor

• Primary Device ID: 04038653462650
• NIH Device Record Key: 9ca98c18-9387-4d37-93c7-e43911a65d89
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Biolox® Option
• Version Model Number: NJ437T
• Catalog Number: NJ437T
• Company DUNS: 315018218
• Company Name: Aesculap AG
• 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)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04038653462650 [Primary]

FDA Product Code

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

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: 2024-11-20
• Device Publish Date: 2015-09-24

On-Brand Devices [Biolox® Option]

• 04046963182076: BIOLOX DELTA REVISION HEAD 12/14 36MM XL
• 04046963182069: BIOLOX DELTA REVISION HEAD 12/14 36MM L
• 04046963182052: BIOLOX DELTA REVISION HEAD 12/14 36MM M
• 04046963182045: BIOLOX DELTA REVISION HEAD 12/14 36MM S
• 04038653434114: BIOLOX DELTA REVISION HEAD 12/14 32MM XL
• 04038653434107: BIOLOX DELTA REVISION HEAD 12/14 32MM L
• 04038653434091: BIOLOX DELTA REVISION HEAD 12/14 32MM M
• 04038653434084: BIOLOX DELTA REVISION HEAD 12/14 32MM S
• 04038653434077: BIOLOX DELTA REVISION HEAD 12/14 28MM XL
• 04038653434060: BIOLOX DELTA REVISION HEAD 12/14 28MM L
• 04038653434053: BIOLOX DELTA REVISION HEAD 12/14 28MM M
• 04038653434046: BIOLOX DELTA REVISION HEAD 12/14 28MM S
• 04038653462650: SLEEVE 8/10 L F/BIOLOX REVISION HEAD