Cup Reamer Size 52 3700502206739

GUDID 07630055300232

Acetabular reamer ø53mm for implant cup ø52mm

Incipio Devices SA

Acetabular orthopaedic reamer

• Primary Device ID: 07630055300232
• NIH Device Record Key: d64482b7-3824-404b-abbf-54d0d5259d99
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cup Reamer Size 52
• Version Model Number: 3700502206739
• Catalog Number: 3700502206739
• Company DUNS: 485098284
• Company Name: Incipio Devices SA
• 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

Device Dimensions

• Outer Diameter: 53 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07630055300232 [Primary]

FDA Product Code

• HTO: Reamer

Sterilization

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

[07630055300232]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-03
• Device Publish Date: 2019-12-26

On-Brand Devices [Cup Reamer Size 52]

• 07630055300232: Acetabular reamer ø53mm for implant cup ø52mm
• 07630055304285: Acetabular reamer ø53mm for implant cup ø52mm