Spirobank II Light (UDI 08052990320455)
Manufactured by MIR - Medical International Research S.p.A.
Device Regulatory Overview
The Spirobank II Light (Model/Catalog Number: 914022) 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
- 914022
- Product Code / EMDN
- Z12150102
- Device Name
- MIR102
- Database Sync Date
- 2026-08-09 17:05:34
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Spirobank II Light?
The registered manufacturer of record for Spirobank II Light is MIR - Medical International Research S.p.A..
What is the Primary UDI-DI identifier for Spirobank II Light?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052990320455.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint