eudamed_udi
Primary ID: 87201657931504
Unspecified Brand (UDI 87201657931504)
Manufactured by Patiënt Lifting Solutions bv
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 87201657931504
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 1001) is a medical device manufactured by Patiënt Lifting Solutions bv. This product is indexed under FDA Product Code / Category Classification V08050302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1001
- Product Code / EMDN
- V08050302
- Device Name
- Track Turntable
- Database Sync Date
- 2026-08-09 16:47:33
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Patiënt Lifting Solutions bv.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 87201657931504.
What classification code is assigned to this device?
This device is registered under product classification code V08050302.
Similar Classification Devices (V08050302)
Other Devices by Patiënt Lifting Solutions bv
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint