eudamed_udi
Primary ID: 08720299493964
Van Raam (UDI 08720299493964)
Manufactured by Van Raam Reha Bikes B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Van Raam - Primary ID 08720299493964
Device Regulatory Overview
The Van Raam (Model/Catalog Number: 388-XXXX) is a medical device manufactured by Van Raam Reha Bikes B.V.. This product is indexed under FDA Product Code / Category Classification Y121801 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 388-XXXX
- Product Code / EMDN
- Y121801
- Device Name
- Balance 2
- Database Sync Date
- 2026-08-09 16:29:12
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 Van Raam?
The registered manufacturer of record for Van Raam is Van Raam Reha Bikes B.V..
What is the Primary UDI-DI identifier for Van Raam?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720299493964.
What classification code is assigned to this device?
This device is registered under product classification code Y121801.
Similar Classification Devices (Y121801)
Other Devices by Van Raam Reha Bikes B.V.
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