Bone Wax White (UDI 902)
Manufactured by Surgical Specialties Mxico, S. de R.L. de C.V.
Device Regulatory Overview
The Bone Wax White (Model/Catalog Number: 902) is a medical device manufactured by Surgical Specialties Mxico, S. de R.L. de C.V.. This product is indexed under FDA Product Code / Category Classification MTJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 902
- Product Code / EMDN
- MTJ
- Device Name
- Bone Wax White
- Database Sync Date
- 2026-08-09 09:35:53
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 White?
The registered manufacturer of record for Bone Wax White is Surgical Specialties Mxico, S. de R.L. de C.V..
What is the Primary UDI-DI identifier for Bone Wax White?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 902.
What classification code is assigned to this device?
This device is registered under product classification code MTJ.
Similar Classification Devices (MTJ)
Other Devices by Surgical Specialties Mxico, S. de R.L. de C.V.
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