eudamed_udi
Primary ID: 08437023168042
MULETILLA (UDI 08437023168042)
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 MULETILLA - Primary ID 08437023168042
Device Regulatory Overview
The MULETILLA (Model/Catalog Number: 0101) is a medical device manufactured by EUROBASTON, S.L. - NIF B33851155. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0101
- Product Code / EMDN
- Y12030601
- Device Name
- BASTON
- Database Sync Date
- 2026-08-09 18:25:36
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 MULETILLA?
The registered manufacturer of record for MULETILLA is EUROBASTON, S.L. - NIF B33851155.
What is the Primary UDI-DI identifier for MULETILLA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437023168042.
What classification code is assigned to this device?
This device is registered under product classification code Y12030601.
Similar Classification Devices (Y12030601)
Other Devices by EUROBASTON, S.L. - NIF B33851155
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