GUDIDData
eudamed_udi Primary ID: 08720261260501

Suelo (UDI 08720261260501)

Manufactured by Nijland Cycling B.V.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Suelo - Primary ID 08720261260501

Device Regulatory Overview

The Suelo (Model/Catalog Number: 111181/111182/111183/111184) is a medical device manufactured by Nijland Cycling B.V.. This product is indexed under FDA Product Code / Category Classification Y121806 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
111181/111182/111183/111184
Product Code / EMDN
Y121806
Device Name
Two Wheel Bikes
Database Sync Date
2026-08-09 16:46:04

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Suelo?

The registered manufacturer of record for Suelo is Nijland Cycling B.V..

What is the Primary UDI-DI identifier for Suelo?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720261260501.

What classification code is assigned to this device?

This device is registered under product classification code Y121806.

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