Hook, medium 1908-5202

GUDID 04719872156161

Hook, medium

UNITED ORTHOPEDIC CORP.

Acetabular shell

• Primary Device ID: 04719872156161
• NIH Device Record Key: 16a61be1-279a-440d-8a67-7fa5a20fbe64
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hook, medium
• Version Model Number: 1908-5202
• Catalog Number: 1908-5202
• 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
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw
• Phone: +886229294567
• Email: service@uoc.com.tw

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 Identifiers

Device Issuing Agency	Device ID
GS1	04719872156161 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163441

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: 4
• Public Version Date: 2018-08-08
• Device Publish Date: 2017-10-06

Devices Manufactured by UNITED ORTHOPEDIC CORP.

• 04719886912524 - Locking Cage: 2026-03-11 Locking cage tray, #1
• 04719886912951 - Locking Cage: 2026-03-11 Locking cage trial, OD50mm, left
• 04719886912968 - Locking Cage: 2026-03-11 Locking cage trial, OD54mm, left
• 04719886912975 - Locking Cage: 2026-03-11 Locking cage trial, OD58mm, left
• 04719886912982 - Locking Cage: 2026-03-11 Locking cage trial, OD62mm, left
• 04719886912999 - Locking Cage: 2026-03-11 Locking cage trial, OD66mm, left
• 04719886913002 - Locking Cage: 2026-03-11 Locking cage trial, OD70mm, left
• 04719886913019 - Locking Cage: 2026-03-11 Locking cage trial, OD50mm, right