eudamed_udi
Primary ID: 08436591370765
CE-2150-ARPC (UDI 08436591370765)
Manufactured by MOBERCAS SL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CE-2150-ARPC - Primary ID 08436591370765
Device Regulatory Overview
The CE-2150-ARPC (Model/Catalog Number: CE-2150-ARPC) is a medical device manufactured by MOBERCAS SL. This product is indexed under FDA Product Code / Category Classification V08050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CE-2150-ARPC
- Product Code / EMDN
- V08050101
- Device Name
- CE-2150-ARPC
- Database Sync Date
- 2026-08-09 16:28:46
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 CE-2150-ARPC?
The registered manufacturer of record for CE-2150-ARPC is MOBERCAS SL.
What is the Primary UDI-DI identifier for CE-2150-ARPC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436591370765.
What classification code is assigned to this device?
This device is registered under product classification code V08050101.
Similar Classification Devices (V08050101)
Other Devices by MOBERCAS SL
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