eudamed_udi
Primary ID: 05902186021242
SPRINT 2 (UDI 05902186021242)
Manufactured by TORUSCARE Sp. z o.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SPRINT 2 - Primary ID 05902186021242
Device Regulatory Overview
The SPRINT 2 (Model/Catalog Number: FS1855022BC) is a medical device manufactured by TORUSCARE Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification V08050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FS1855022BC
- Product Code / EMDN
- V08050101
- Device Name
- Stretcher
- Database Sync Date
- 2026-08-09 16:29:58
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 SPRINT 2?
The registered manufacturer of record for SPRINT 2 is TORUSCARE Sp. z o.o..
What is the Primary UDI-DI identifier for SPRINT 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05902186021242.
What classification code is assigned to this device?
This device is registered under product classification code V08050101.
Similar Classification Devices (V08050101)
Other Devices by TORUSCARE Sp. z o.o.
Programmatic Export
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