DM Acetabular System 1207-2628

GUDID 04719872143215

DM Liner trial adapter, 28/22

UNITED ORTHOPEDIC CORP.

Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable

• Primary Device ID: 04719872143215
• NIH Device Record Key: 51c3b927-d9c8-4b73-809e-e17a563586e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DM Acetabular System
• Version Model Number: 1207-2628
• Catalog Number: 1207-2628
• 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
• 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	04719872143215 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

[04719872143215]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-29
• Device Publish Date: 2022-11-21

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