gudid
Primary ID: SPO25
Vitalcontrol (UDI SPO25)
Manufactured by BEURER NORTH AMERICA, L.P.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vitalcontrol - Primary ID SPO25
Device Regulatory Overview
The Vitalcontrol (Model/Catalog Number: SPO25) is a medical device manufactured by BEURER NORTH AMERICA, L.P.. This product is indexed under FDA Product Code / Category Classification PGJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SPO25
- Product Code / EMDN
- PGJ
- Device Name
- SPO25 Pulse OximeterEAN 4066299453886Art. No 453.88
- Database Sync Date
- 2026-08-09 09:37:45
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 Vitalcontrol?
The registered manufacturer of record for Vitalcontrol is BEURER NORTH AMERICA, L.P..
What is the Primary UDI-DI identifier for Vitalcontrol?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SPO25.
What classification code is assigned to this device?
This device is registered under product classification code PGJ.
Similar Classification Devices (PGJ)
Other Devices by BEURER NORTH AMERICA, L.P.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint