GUDIDData
eudamed_udi Primary ID: 05213016041263

ELECTRIC BATH LIFT CHAIR “SPLASH”   (UDI 05213016041263)

Manufactured by ΜΟΝΑΔΑ ΒΙΟΜΗΧΑΝΙΚΩΝ ΙΑΤΡΙΚΩΝ ΑΕΡΙΩΝ ΚΡΗΤΗΣ (ΜΟΒΙΑΚ Α.Ε)

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELECTRIC BATH LIFT CHAIR “SPLASH”   - Primary ID 05213016041263

Device Regulatory Overview

The ELECTRIC BATH LIFT CHAIR “SPLASH”   (Model/Catalog Number: 0815720) is a medical device manufactured by ΜΟΝΑΔΑ ΒΙΟΜΗΧΑΝΙΚΩΝ ΙΑΤΡΙΚΩΝ ΑΕΡΙΩΝ ΚΡΗΤΗΣ (ΜΟΒΙΑΚ Α.Ε). This product is indexed under FDA Product Code / Category Classification Y183099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0815720
Product Code / EMDN
Y183099
Device Name
LIFT CHAIR
Database Sync Date
2026-08-09 17:18:11

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 ELECTRIC BATH LIFT CHAIR “SPLASH”  ?

The registered manufacturer of record for ELECTRIC BATH LIFT CHAIR “SPLASH”   is ΜΟΝΑΔΑ ΒΙΟΜΗΧΑΝΙΚΩΝ ΙΑΤΡΙΚΩΝ ΑΕΡΙΩΝ ΚΡΗΤΗΣ (ΜΟΒΙΑΚ Α.Ε).

What is the Primary UDI-DI identifier for ELECTRIC BATH LIFT CHAIR “SPLASH”  ?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213016041263.

What classification code is assigned to this device?

This device is registered under product classification code Y183099.

Similar Classification Devices (Y183099)

Other Devices by ΜΟΝΑΔΑ ΒΙΟΜΗΧΑΝΙΚΩΝ ΙΑΤΡΙΚΩΝ ΑΕΡΙΩΝ ΚΡΗΤΗΣ (ΜΟΒΙΑΚ Α.Ε)

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