Delta PF Cup 9055.51.040

GUDID 08033390071871

Adapter Small for Curved Impactor

LIMACORPORATE SPA

Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable Orthopaedic implant impactor, reusable

• Primary Device ID: 08033390071871
• NIH Device Record Key: f67f92eb-97e9-4d00-b871-095c77c4faff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Delta PF Cup
• Version Model Number: Adapter
• Catalog Number: 9055.51.040
• Company DUNS: 432066322
• Company Name: LIMACORPORATE SPA
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

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 Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033390071871 [Primary]

FDA Product Code

• MBL: Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous

Sterilization

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

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

[08033390071871]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2024-01-08
• Device Publish Date: 2016-08-04

On-Brand Devices [Delta PF Cup]

• 08033390071901: Trial Adapter for Curved Impactor
• 08033390071864: Alignment Jig for Curved Impactor
• 08033390071895: Adapter Large for Curved Impactor
• 08033390071888: Adapter Medium for Curved Impactor
• 08033390071871: Adapter Small for Curved Impactor
• 08033390063357: Adapter Large for Cups Wrench
• 08033390063340: Adapter Medium for Cups Wrench
• 08033390063333: Adapter Small for Cups Wrench
• 08033390025409: Wrench for Cups