eudamed_udi
Primary ID: 08437023168400
Tubular velcro 32 (UDI 08437023168400)
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 Tubular velcro 32 - Primary ID 08437023168400
Device Regulatory Overview
The Tubular velcro 32 (Model/Catalog Number: 02832) is a medical device manufactured by EUROBASTON, S.L. - NIF B33851155. This product is indexed under FDA Product Code / Category Classification Y060399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02832
- Product Code / EMDN
- Y060399
- Device Name
- FAJAS
- Database Sync Date
- 2026-08-09 17:32:05
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 Tubular velcro 32?
The registered manufacturer of record for Tubular velcro 32 is EUROBASTON, S.L. - NIF B33851155.
What is the Primary UDI-DI identifier for Tubular velcro 32?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437023168400.
What classification code is assigned to this device?
This device is registered under product classification code Y060399.
Similar Classification Devices (Y060399)
Other Devices by EUROBASTON, S.L. - NIF B33851155
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