Spirolab Plus (UDI 08052990322121)
Manufactured by MIR - Medical International Research S.p.A.
Device Regulatory Overview
The Spirolab Plus (Model/Catalog Number: 904030) is a medical device manufactured by MIR - Medical International Research S.p.A.. This product is indexed under FDA Product Code / Category Classification Z12150102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 904030
- Product Code / EMDN
- Z12150102
- Device Name
- MIR100
- Database Sync Date
- 2026-08-09 17:30:33
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 Spirolab Plus?
The registered manufacturer of record for Spirolab Plus is MIR - Medical International Research S.p.A..
What is the Primary UDI-DI identifier for Spirolab Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052990322121.
What classification code is assigned to this device?
This device is registered under product classification code Z12150102.
Similar Classification Devices (Z12150102)
Other Devices by MIR - Medical International Research S.p.A.
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