gudid
Primary ID: WW390F
CONAIR (UDI WW390F)
Manufactured by CONAIR CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CONAIR - Primary ID WW390F
Device Regulatory Overview
The CONAIR (Model/Catalog Number: WW390F) is a medical device manufactured by CONAIR CORPORATION. This product is indexed under FDA Product Code / Category Classification MNW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WW390F
- Product Code / EMDN
- MNW
- Device Name
- BMI Scale
- Database Sync Date
- 2026-08-09 09:08:47
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 CONAIR?
The registered manufacturer of record for CONAIR is CONAIR CORPORATION.
What is the Primary UDI-DI identifier for CONAIR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WW390F.
What classification code is assigned to this device?
This device is registered under product classification code MNW.
Similar Classification Devices (MNW)
Other Devices by CONAIR CORPORATION
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