DM Acetabular System

GUDID 04719872141785

Flange bender

UNITED ORTHOPEDIC CORP.

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 04719872141785
• NIH Device Record Key: 0fd5b993-236d-4ff6-bbb3-bf0b22274ccf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DM Acetabular System
• Version Model Number: 9207-5106
• 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: 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
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	04719872141785 [Primary]

FDA Product Code

• HTW: Bit, Drill

Sterilization

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

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

[04719872141785]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-07-31
• Device Publish Date: 2020-07-23

On-Brand Devices [DM Acetabular System]

• 04719872141785: Flange bender
• 04719872141778: Flexible peg drill
• 04719872141761: Holder shaft
• 04719872141754: Drill guide, peg
• 04719872141747: Cup trial handle
• 04719872145295: Peg dilator, curved
• 04719872145288: Peg dilator, offset
• 04719872145240: Peg punch, curved
• 04719872145233: Peg punch, offset
• 04719872145226: Peg punch, angled
• 04719872145219: Peg inserter, curved
• 04719872143291: Peg inserter, offset
• 04719872143284: Peg inserter, angled
• 04719872143246: Cup positioner, offset
• 04719872143239: Cup positioner, straight
• 04719872142287: Peg remover guide
• 04719872142270: DM Cup flange drill guide, Ø3.2mm
• 04719872143413: Cup holder adaptor, OD52mm
• 04719872143406: Cup holder adaptor, OD50mm
• 04719872143390: Cup holder adaptor, OD48mm
• 04719872143383: Cup holder adaptor, OD46mm
• 04719872143376: Cup holder adaptor, OD44mm
• 04719872143369: Cup holder adaptor, OD42mm
• 04719872143307: DM Liner holder
• 04719872143253: DM Press
• 04719872142300: Press baseplate
• 04719872142294: Peg remover
• 04719872143499: Cup holder adaptor, OD68mm
• 04719872143482: Cup holder adaptor, OD66mm
• 04719872143475: Cup holder adaptor, OD64mm
• 04719872143468: Cup holder adaptor, OD62mm
• 04719872143451: Cup holder adaptor, OD60mm
• 04719872143444: Cup holder adaptor, OD58mm
• 04719872143437: Cup holder adaptor, OD56mm
• 04719872143420: Cup holder adaptor, OD54mm
• 04719886893229: Cup positioner, offset
• 04719886890808: Cup positioner, offset
• 04719872143215: DM Liner trial adapter, 28/22
• 04719886894493: Cup trial adaptor
• 04719886900293: Cup positioner, offset
• 04719886900286: Cup positioner, offset
• 04719886900279: Cup positioner, straight