Triathlon (UDI 07613327241464)
Manufactured by Howmedica Osteonics Corp.
Device Regulatory Overview
The Triathlon (Model/Catalog Number: 6541-3-524) is a medical device manufactured by Howmedica Osteonics Corp.. This product is indexed under FDA Product Code / Category Classification L0917 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 6541-3-524
- Product Code / EMDN
- L0917
- Device Name
- TF-019 Class IIa - Drill Bit
- Database Sync Date
- 2026-08-09 16:49:47
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Triathlon?
The registered manufacturer of record for Triathlon is Howmedica Osteonics Corp..
What is the Primary UDI-DI identifier for Triathlon?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613327241464.
What classification code is assigned to this device?
This device is registered under product classification code L0917.
Similar Classification Devices (L0917)
Other Devices by Howmedica Osteonics Corp.
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