gudid
Primary ID: E5020
SpiroFlow (UDI E5020)
Manufactured by Spirometrics
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SpiroFlow - Primary ID E5020
Device Regulatory Overview
The SpiroFlow (Model/Catalog Number: E5020) is a medical device manufactured by Spirometrics. This product is indexed under FDA Product Code / Category Classification BZH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E5020
- Product Code / EMDN
- BZH
- Device Name
- Child Peak Flow Meter
- Database Sync Date
- 2026-08-09 09:49:29
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 SpiroFlow?
The registered manufacturer of record for SpiroFlow is Spirometrics.
What is the Primary UDI-DI identifier for SpiroFlow?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E5020.
What classification code is assigned to this device?
This device is registered under product classification code BZH.
Similar Classification Devices (BZH)
Other Devices by Spirometrics
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint