eudamed_udi
Primary ID: 08437023168240
CABESTRILLO RATIER (UDI 08437023168240)
Manufactured by EUROBASTON, S.L. - NIF B33851155
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CABESTRILLO RATIER - Primary ID 08437023168240
Device Regulatory Overview
The CABESTRILLO RATIER (Model/Catalog Number: 02146) is a medical device manufactured by EUROBASTON, S.L. - NIF B33851155. This product is indexed under FDA Product Code / Category Classification M030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02146
- Product Code / EMDN
- M030501
- Device Name
- Cabestrillo
- Database Sync Date
- 2026-08-09 16:46:49
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 CABESTRILLO RATIER?
The registered manufacturer of record for CABESTRILLO RATIER is EUROBASTON, S.L. - NIF B33851155.
What is the Primary UDI-DI identifier for CABESTRILLO RATIER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437023168240.
What classification code is assigned to this device?
This device is registered under product classification code M030501.
Similar Classification Devices (M030501)
Other Devices by EUROBASTON, S.L. - NIF B33851155
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