Hook, small 1908-5201

GUDID 04719872154532

Hook, small

UNITED ORTHOPEDIC CORP.

Acetabular shell

• Primary Device ID: 04719872154532
• NIH Device Record Key: 3cdeeecd-4c8d-4faa-951a-efd890b5f5bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hook, small
• Version Model Number: 1908-5201
• Catalog Number: 1908-5201
• 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	04719872154532 [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.

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• 04719886895841 - Resolve Modular Revision Hip Stem: 2025-05-21 Resolve Distal Stem, Interlocking, Ø17×220mm
• 04719886895858 - Resolve Modular Revision Hip Stem: 2025-05-21 Resolve Distal Stem, Interlocking, Ø18×220mm
• 04719886895865 - Resolve Modular Revision Hip Stem: 2025-05-21 Resolve Distal Stem, Interlocking, Ø19×220mm
• 04719886895872 - Resolve Modular Revision Hip Stem: 2025-05-21 Resolve Distal Stem, Interlocking, Ø20×220mm
• 04719886895889 - Resolve Modular Revision Hip Stem: 2025-05-21 Resolve Distal Stem, Interlocking, Ø21×220mm
• 04719886895896 - Resolve Modular Revision Hip Stem: 2025-05-21 Resolve Distal Stem, Interlocking, Ø22×220mm