eudamed_udi Primary ID: 07640156393897

WF-5000 Non-contact infrared thermometer (UDI 07640156393897)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The WF-5000 Non-contact infrared thermometer (Model/Catalog Number: 1101312) is a medical device manufactured by B.Well Swiss AG. This product is indexed under FDA Product Code / Category Classification V0301010202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1101312
Product Code / EMDN: V0301010202
Device Name: Non-contact infrared thermometer
Database Sync Date: 2026-08-09 18:17:16

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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Frequently Asked Questions

Who is the primary manufacturer of WF-5000 Non-contact infrared thermometer?

The registered manufacturer of record for WF-5000 Non-contact infrared thermometer is B.Well Swiss AG.

What is the Primary UDI-DI identifier for WF-5000 Non-contact infrared thermometer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640156393897.

What classification code is assigned to this device?

This device is registered under product classification code V0301010202.

Similar Classification Devices (V0301010202)

Other Devices by B.Well Swiss AG

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