gudid
Primary ID: 32910004
Sunbeam (UDI 32910004)
Manufactured by Star Elite Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sunbeam - Primary ID 32910004
Device Regulatory Overview
The Sunbeam (Model/Catalog Number: 32910004) is a medical device manufactured by Star Elite Inc. This product is indexed under FDA Product Code / Category Classification MNW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 32910004
- Product Code / EMDN
- MNW
- Device Name
- Body analysis scale
- Database Sync Date
- 2026-08-09 09:04:20
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 Sunbeam?
The registered manufacturer of record for Sunbeam is Star Elite Inc.
What is the Primary UDI-DI identifier for Sunbeam?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 32910004.
What classification code is assigned to this device?
This device is registered under product classification code MNW.
Similar Classification Devices (MNW)
Other Devices by Star Elite Inc
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