Spirometer (UDI 06958066408084)
Manufactured by Suzhou Beneware Medical Equipment Co.,Ltd.
Device Regulatory Overview
The Spirometer (Model/Catalog Number: SP-02-EN) is a medical device manufactured by Suzhou Beneware Medical Equipment Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification Z12150101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SP-02-EN
- Product Code / EMDN
- Z12150101
- Device Name
- Spirometer systems
- Database Sync Date
- 2026-08-09 17:56:34
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 Spirometer?
The registered manufacturer of record for Spirometer is Suzhou Beneware Medical Equipment Co.,Ltd..
What is the Primary UDI-DI identifier for Spirometer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958066408084.
What classification code is assigned to this device?
This device is registered under product classification code Z12150101.
Similar Classification Devices (Z12150101)
Other Devices by Suzhou Beneware Medical Equipment Co.,Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint