gudid
Primary ID: RX DC
NewTom (UDI RX DC)
Manufactured by CEFLA SOCIETA' COOPERATIVA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NewTom - Primary ID RX DC
Device Regulatory Overview
The NewTom (Model/Catalog Number: RX DC) is a medical device manufactured by CEFLA SOCIETA' COOPERATIVA. This product is indexed under FDA Product Code / Category Classification EHD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RX DC
- Product Code / EMDN
- EHD
- Device Name
- NEWTOM RX DC - REF: NMEU174WS
- Database Sync Date
- 2026-08-09 09:04:34
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 NewTom?
The registered manufacturer of record for NewTom is CEFLA SOCIETA' COOPERATIVA.
What is the Primary UDI-DI identifier for NewTom?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RX DC.
What classification code is assigned to this device?
This device is registered under product classification code EHD.
Similar Classification Devices (EHD)
Other Devices by CEFLA SOCIETA' COOPERATIVA
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