9901-8103-RA

GUDID 04719886911190

Universal tray

UNITED ORTHOPEDIC CORP.

Instrument tray, reusable

• Primary Device ID: 04719886911190
• NIH Device Record Key: f9ee213b-369a-4fe1-a414-1817afc9ef41
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 9901-8103-RA
• Catalog Number: 9901-8103-RA
• Company DUNS: 656700556
• Company Name: UNITED ORTHOPEDIC CORP.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com
• Phone: +886229294567
• Email: tw.service@unitedorthopedic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04719886911190 [Primary]

FDA Product Code

• FSM: Tray, Surgical, Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

[04719886911190]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-01-14
• Device Publish Date: 2026-01-06

Devices Manufactured by UNITED ORTHOPEDIC CORP.

• 04719886911190 - NA: 2026-01-14Universal tray
• 04719886911190 - NA: 2026-01-14 Universal tray
• 04719886912180 - Resolve Modular Revision Stem: 2026-01-14 Resolve proximal component trial, Ø19×55mm
• 04719886912197 - Resolve Modular Revision Stem: 2026-01-14 Resolve proximal component trial, Ø19×65mm
• 04719886912203 - Resolve Modular Revision Stem: 2026-01-14 Resolve proximal component trial, Ø21×65mm
• 04719886912210 - Resolve Modular Revision Stem: 2026-01-14 Resolve proximal component trial, Ø23×65mm
• 04719886912227 - Resolve Modular Revision Stem: 2026-01-14 Resolve proximal component trial, Ø25×65mm
• 04719886912234 - Resolve Modular Revision Stem: 2026-01-14 Resolve proximal component trial, Ø19×75mm
• 04719886912241 - Resolve Modular Revision Stem: 2026-01-14 Resolve proximal component trial, Ø21×75mm