MDI Spacer PLUS, 220 ml, adult (UDI 04716770383002)
Manufactured by Besmed Health Business Corp.
Device Regulatory Overview
The MDI Spacer PLUS, 220 ml, adult (Model/Catalog Number: MD-38300) is a medical device manufactured by Besmed Health Business Corp.. This product is indexed under FDA Product Code / Category Classification R03010302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MD-38300
- Product Code / EMDN
- R03010302
- Device Name
- MDI Spacer, Silicone mask, 220 ml, adult
- Database Sync Date
- 2026-08-09 17:26:04
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 MDI Spacer PLUS, 220 ml, adult?
The registered manufacturer of record for MDI Spacer PLUS, 220 ml, adult is Besmed Health Business Corp..
What is the Primary UDI-DI identifier for MDI Spacer PLUS, 220 ml, adult?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04716770383002.
What classification code is assigned to this device?
This device is registered under product classification code R03010302.
Similar Classification Devices (R03010302)
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