Spirodoc (UDI 08052990320356)
Manufactured by MIR - Medical International Research S.p.A.
Device Regulatory Overview
The Spirodoc (Model/Catalog Number: 910606 - 910606E - 910606I) is a medical device manufactured by MIR - Medical International Research S.p.A.. This product is indexed under FDA Product Code / Category Classification Z1203020408 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 910606 - 910606E - 910606I
- Product Code / EMDN
- Z1203020408
- Device Name
- MIR040
- Database Sync Date
- 2026-08-09 16:29:02
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 Spirodoc?
The registered manufacturer of record for Spirodoc is MIR - Medical International Research S.p.A..
What is the Primary UDI-DI identifier for Spirodoc?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052990320356.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020408.
Similar Classification Devices (Z1203020408)
Other Devices by MIR - Medical International Research S.p.A.
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