gudid
Primary ID: R & S SupraSpeed+
R & S (UDI R & S SupraSpeed+)
Manufactured by LARES RESEARCH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for R & S - Primary ID R & S SupraSpeed+
Device Regulatory Overview
The R & S (Model/Catalog Number: R & S SupraSpeed+) is a medical device manufactured by LARES RESEARCH. This product is indexed under FDA Product Code / Category Classification EFB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R & S SupraSpeed+
- Product Code / EMDN
- EFB
- Device Name
- R & S Supraspeed+ Pushbutton Ceramic ball bearing
- Database Sync Date
- 2026-08-09 09:01:11
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 R & S?
The registered manufacturer of record for R & S is LARES RESEARCH.
What is the Primary UDI-DI identifier for R & S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R & S SupraSpeed+.
What classification code is assigned to this device?
This device is registered under product classification code EFB.
Similar Classification Devices (EFB)
Other Devices by LARES RESEARCH
Programmatic Export
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