GUDIDData
eudamed_udi Primary ID: 05904804646066

VELMOR 3 MAX bateria litowo-jonowa żółty (UDI 05904804646066)

Manufactured by BILI BIKE SP. Z O.O.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VELMOR 3 MAX bateria litowo-jonowa żółty - Primary ID 05904804646066

Device Regulatory Overview

The VELMOR 3 MAX bateria litowo-jonowa żółty (Model/Catalog Number: BBSKUTER1923) is a medical device manufactured by BILI BIKE SP. Z O.O.. This product is indexed under FDA Product Code / Category Classification Y122124 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BBSKUTER1923
Product Code / EMDN
Y122124
Device Name
Pojazdy elektryczne do transportu medycznego
Database Sync Date
2026-08-09 16:30:27

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 VELMOR 3 MAX bateria litowo-jonowa żółty?

The registered manufacturer of record for VELMOR 3 MAX bateria litowo-jonowa żółty is BILI BIKE SP. Z O.O..

What is the Primary UDI-DI identifier for VELMOR 3 MAX bateria litowo-jonowa żółty?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904804646066.

What classification code is assigned to this device?

This device is registered under product classification code Y122124.

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