eudamed_udi
Primary ID: 04895272901638
Scooter (UDI 04895272901638)
Manufactured by INTCO MEDICAL (HK) CO., ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Scooter - Primary ID 04895272901638
Device Regulatory Overview
The Scooter (Model/Catalog Number: PLAZA Elite Max) is a medical device manufactured by INTCO MEDICAL (HK) CO., ltd. This product is indexed under FDA Product Code / Category Classification Y122124 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PLAZA Elite Max
- Product Code / EMDN
- Y122124
- Device Name
- scooter
- Database Sync Date
- 2026-08-09 16:29:54
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 Scooter?
The registered manufacturer of record for Scooter is INTCO MEDICAL (HK) CO., ltd.
What is the Primary UDI-DI identifier for Scooter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04895272901638.
What classification code is assigned to this device?
This device is registered under product classification code Y122124.
Similar Classification Devices (Y122124)
Other Devices by INTCO MEDICAL (HK) CO., ltd
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