gudid
Primary ID: BW810XL
MERIL - BONEWAX (UDI BW810XL)
Manufactured by MERIL ENDO SURGERY PRIVATE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MERIL - BONEWAX - Primary ID BW810XL
Device Regulatory Overview
The MERIL - BONEWAX (Model/Catalog Number: BW810XL) is a medical device manufactured by MERIL ENDO SURGERY PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification MTJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BW810XL
- Product Code / EMDN
- MTJ
- Device Name
- BONEWAX X 2.5 GM
- Database Sync Date
- 2026-08-09 09:29:39
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MERIL - BONEWAX?
The registered manufacturer of record for MERIL - BONEWAX is MERIL ENDO SURGERY PRIVATE LIMITED.
What is the Primary UDI-DI identifier for MERIL - BONEWAX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BW810XL.
What classification code is assigned to this device?
This device is registered under product classification code MTJ.
Similar Classification Devices (MTJ)
Other Devices by MERIL ENDO SURGERY PRIVATE LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint