gudid
Primary ID: mSpirometer
COHERO (UDI mSpirometer)
Manufactured by MIR MEDICAL INTERNATIONAL RESEARCH SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COHERO - Primary ID mSpirometer
Device Regulatory Overview
The COHERO (Model/Catalog Number: mSpirometer) is a medical device manufactured by MIR MEDICAL INTERNATIONAL RESEARCH SPA. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- mSpirometer
- Product Code / EMDN
- BZG
- Device Name
- Smart Spirometer connected to an app available on a smart phone
- Database Sync Date
- 2026-08-09 09:04:32
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 COHERO?
The registered manufacturer of record for COHERO is MIR MEDICAL INTERNATIONAL RESEARCH SPA.
What is the Primary UDI-DI identifier for COHERO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is mSpirometer.
What classification code is assigned to this device?
This device is registered under product classification code BZG.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint