BM (UDI 06974269382297)
Manufactured by ZHEJIANG BAITE MEDICAL APPLIANCES CO., LTD.
Device Regulatory Overview
The BM (Model/Catalog Number: BM0905) is a medical device manufactured by ZHEJIANG BAITE MEDICAL APPLIANCES CO., LTD.. This product is indexed under FDA Product Code / Category Classification R03010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BM0905
- Product Code / EMDN
- R03010301
- Device Name
- nebulizer mask
- Database Sync Date
- 2026-08-09 16:28:55
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?
The registered manufacturer of record for BM is ZHEJIANG BAITE MEDICAL APPLIANCES CO., LTD..
What is the Primary UDI-DI identifier for BM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974269382297.
What classification code is assigned to this device?
This device is registered under product classification code R03010301.
Similar Classification Devices (R03010301)
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