eudamed_udi
Primary ID: 07640156394825
PRO-39 Wrist blood pressure monitor (UDI 07640156394825)
Manufactured by B.Well Swiss AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PRO-39 Wrist blood pressure monitor - Primary ID 07640156394825
Device Regulatory Overview
The PRO-39 Wrist blood pressure monitor (Model/Catalog Number: 1101236) is a medical device manufactured by B.Well Swiss AG. This product is indexed under FDA Product Code / Category Classification Z1203020302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1101236
- Product Code / EMDN
- Z1203020302
- Device Name
- Blood Pressure Monitor
- Database Sync Date
- 2026-08-09 17:41:45
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 PRO-39 Wrist blood pressure monitor?
The registered manufacturer of record for PRO-39 Wrist blood pressure monitor is B.Well Swiss AG.
What is the Primary UDI-DI identifier for PRO-39 Wrist blood pressure monitor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640156394825.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020302.
Similar Classification Devices (Z1203020302)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint