eudamed_udi
Primary ID: 08470001532510
ACOFAR (UDI 08470001532510)
Manufactured by Eurosirel Spa
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACOFAR - Primary ID 08470001532510
Device Regulatory Overview
The ACOFAR (Model/Catalog Number: RCT532510) is a medical device manufactured by Eurosirel Spa. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RCT532510
- Product Code / EMDN
- M050101
- Device Name
- CLOTH ROLL
- Database Sync Date
- 2026-08-09 16:30:20
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 ACOFAR?
The registered manufacturer of record for ACOFAR is Eurosirel Spa.
What is the Primary UDI-DI identifier for ACOFAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08470001532510.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by Eurosirel Spa
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