BM Silicone Laryngeal Mask Devices (UDI 06942382610726)
Manufactured by Bonree Medical Co., Ltd.
Device Regulatory Overview
The BM Silicone Laryngeal Mask Devices (Model/Catalog Number: 231 03 00 2) is a medical device manufactured by Bonree Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R01020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 231 03 00 2
- Product Code / EMDN
- R01020101
- Device Name
- Laryngeal Mask Devices
- Database Sync Date
- 2026-08-09 16:28:51
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 BM Silicone Laryngeal Mask Devices?
The registered manufacturer of record for BM Silicone Laryngeal Mask Devices is Bonree Medical Co., Ltd..
What is the Primary UDI-DI identifier for BM Silicone Laryngeal Mask Devices?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942382610726.
What classification code is assigned to this device?
This device is registered under product classification code R01020101.
Similar Classification Devices (R01020101)
Other Devices by Bonree Medical Co., Ltd.
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