banda adhesiva codera (UDI 08437023168448)
Manufactured by EUROBASTON, S.L. - NIF B33851155
Device Regulatory Overview
The banda adhesiva codera (Model/Catalog Number: 02720) is a medical device manufactured by EUROBASTON, S.L. - NIF B33851155. This product is indexed under FDA Product Code / Category Classification M030402010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02720
- Product Code / EMDN
- M030402010101
- Device Name
- BANDAS ELÁSTICAS
- Database Sync Date
- 2026-08-09 17:14:46
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 banda adhesiva codera?
The registered manufacturer of record for banda adhesiva codera is EUROBASTON, S.L. - NIF B33851155.
What is the Primary UDI-DI identifier for banda adhesiva codera?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437023168448.
What classification code is assigned to this device?
This device is registered under product classification code M030402010101.
Similar Classification Devices (M030402010101)
Other Devices by EUROBASTON, S.L. - NIF B33851155
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