eudamed_udi
Primary ID: 08720261260228
Nindo (UDI 08720261260228)
Manufactured by Nijland Cycling B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nindo - Primary ID 08720261260228
Device Regulatory Overview
The Nindo (Model/Catalog Number: 125041/125046) is a medical device manufactured by Nijland Cycling 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
- 125041/125046
- Product Code / EMDN
- Y121801
- Device Name
- Sight Seeing Tandems
- Database Sync Date
- 2026-08-09 17:13:59
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 Nindo?
The registered manufacturer of record for Nindo is Nijland Cycling B.V..
What is the Primary UDI-DI identifier for Nindo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720261260228.
What classification code is assigned to this device?
This device is registered under product classification code Y121801.
Similar Classification Devices (Y121801)
Other Devices by Nijland Cycling B.V.
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