eudamed_udi Primary ID: 08435669518702

BASTON TUKAN NEGRO C/PUÑO NEOPRENO. (UDI 08435669518702)

Manufactured by FABRICACIONES ORTOPEDICAS ALBACETE, S.L.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The BASTON TUKAN NEGRO C/PUÑO NEOPRENO. (Model/Catalog Number: 0101.4511) is a medical device manufactured by FABRICACIONES ORTOPEDICAS ALBACETE, S.L.. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 0101.4511
Product Code / EMDN: Y12030601
Device Name: TUKAN
Database Sync Date: 2026-08-09 16:28:47

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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Frequently Asked Questions

Who is the primary manufacturer of BASTON TUKAN NEGRO C/PUÑO NEOPRENO.?

The registered manufacturer of record for BASTON TUKAN NEGRO C/PUÑO NEOPRENO. is FABRICACIONES ORTOPEDICAS ALBACETE, S.L..

What is the Primary UDI-DI identifier for BASTON TUKAN NEGRO C/PUÑO NEOPRENO.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435669518702.

What classification code is assigned to this device?

This device is registered under product classification code Y12030601.

Similar Classification Devices (Y12030601)

Other Devices by FABRICACIONES ORTOPEDICAS ALBACETE, S.L.

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