gudid
Primary ID: PO30
Beurer (UDI PO30)
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 Beurer - Primary ID PO30
Device Regulatory Overview
The Beurer (Model/Catalog Number: PO30) 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
- PO30
- Product Code / EMDN
- PGJ
- Device Name
- Fingertip Pulse Oximeter (for wellness)
- Database Sync Date
- 2026-08-09 09:49:33
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Beurer?
The registered manufacturer of record for Beurer is BEURER NORTH AMERICA, L.P..
What is the Primary UDI-DI identifier for Beurer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PO30.
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.
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