INSTRUMENT (UDI I-H1236HA00)
Manufactured by Howmedica Osteonics Corp.
Device Regulatory Overview
The INSTRUMENT (Model/Catalog Number: I-H1236HA00) is a medical device manufactured by Howmedica Osteonics Corp.. This product is indexed under FDA Product Code / Category Classification KWL 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
- I-H1236HA00
- Product Code / EMDN
- KWL
- Device Name
- SPECIALTY TRIDENT TRIAL CONTAINMENT SCREW-LONGER
- Database Sync Date
- 2026-08-09 09:21:51
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 INSTRUMENT?
The registered manufacturer of record for INSTRUMENT is Howmedica Osteonics Corp..
What is the Primary UDI-DI identifier for INSTRUMENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is I-H1236HA00.
What classification code is assigned to this device?
This device is registered under product classification code KWL.
Similar Classification Devices (KWL)
Other Devices by Howmedica Osteonics Corp.
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