PROSTALAC 254196000

GUDID 10603295129714

PROSTALAC HIP EXTRACTOR

DEPUY ORTHOPAEDICS, INC.

Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 10603295129714
• NIH Device Record Key: 865f90f3-97ad-49d2-a738-e1a5a0363073
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROSTALAC
• Version Model Number: 2541-96-000
• Catalog Number: 254196000
• Company DUNS: 080506581
• Company Name: DEPUY ORTHOPAEDICS, INC.
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10603295129714 [Primary]

FDA Product Code

• HWB: EXTRACTOR

Sterilization

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

[10603295129714]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-04-23
• Device Publish Date: 2018-09-24

On-Brand Devices [PROSTALAC]

• 10603295129714: PROSTALAC HIP EXTRACTOR
• 10603295129554: PROSTALAC QUICK RELEASE NUT
• 10603295129547: PROSTALAC MOLD JAW
• 10603295129530: PROSTALAC MOLD BASE