U-Motion II XPE Cup liner, 20 degrees, OD50mm, ID3 1406-5651

GUDID 04711605580793

U-Motion II XPE Cup liner, 20 degrees, OD50mm, ID36mm

UNITED ORTHOPEDIC CORP.

Ceramic-on-ceramic total hip prosthesis

• Primary Device ID: 04711605580793
• NIH Device Record Key: fbe987fe-2836-4d14-83b3-b7305b203b57
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: U-Motion II XPE Cup liner, 20 degrees, OD50mm, ID3
• Version Model Number: 1406-5651
• Catalog Number: 1406-5651
• Company DUNS: 656700556
• Company Name: UNITED ORTHOPEDIC CORP.
• 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: +886229294567
• Email: service@uoc.com.tw

Device Dimensions

• Outer Diameter: 50 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04711605580793 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170089

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: 2018-08-07
• Device Publish Date: 2018-04-19

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