Bone Wax (UDI BW25G)
Manufactured by Covidien LP
Device Regulatory Overview
The Bone Wax (Model/Catalog Number: BW25G) is a medical device manufactured by Covidien LP. This product is indexed under FDA Product Code / Category Classification MTJ 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
- BW25G
- Product Code / EMDN
- MTJ
- Device Name
- Bone Wax
- Database Sync Date
- 2026-08-09 10:00:59
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 Bone Wax?
The registered manufacturer of record for Bone Wax is Covidien LP.
What is the Primary UDI-DI identifier for Bone Wax?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BW25G.
What classification code is assigned to this device?
This device is registered under product classification code MTJ.
Similar Classification Devices (MTJ)
Other Devices by Covidien LP
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