gudid
Primary ID: Lexa PLUS RIS-311
Lexa PLUS RIS-311 (UDI Lexa PLUS RIS-311)
Manufactured by W & H STERILIZATION SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lexa PLUS RIS-311 - Primary ID Lexa PLUS RIS-311
Device Regulatory Overview
The Lexa PLUS RIS-311 (Model/Catalog Number: Lexa PLUS RIS-311) is a medical device manufactured by W & H STERILIZATION SRL. This product is indexed under FDA Product Code / Category Classification FLE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Lexa PLUS RIS-311
- Product Code / EMDN
- FLE
- Device Name
- TABLE-TOP STEAM STERILIZER LEXA PLUS RIS-311
- Database Sync Date
- 2026-08-09 09:07:31
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 Lexa PLUS RIS-311?
The registered manufacturer of record for Lexa PLUS RIS-311 is W & H STERILIZATION SRL.
What is the Primary UDI-DI identifier for Lexa PLUS RIS-311?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Lexa PLUS RIS-311.
What classification code is assigned to this device?
This device is registered under product classification code FLE.
Similar Classification Devices (FLE)
Other Devices by W & H STERILIZATION SRL
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