eudamed_udi
Primary ID: 08057760160019
Caress Flow Solution (UDI 08057760160019)
Manufactured by CARESS FLOW Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Caress Flow Solution - Primary ID 08057760160019
Device Regulatory Overview
The Caress Flow Solution (Model/Catalog Number: Caress Flow Solution) is a medical device manufactured by CARESS FLOW Srl. This product is indexed under FDA Product Code / Category Classification U0803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Caress Flow Solution
- Product Code / EMDN
- U0803
- Device Name
- Caress Flow Solution
- Database Sync Date
- 2026-08-09 16:50:55
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 Caress Flow Solution?
The registered manufacturer of record for Caress Flow Solution is CARESS FLOW Srl.
What is the Primary UDI-DI identifier for Caress Flow Solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057760160019.
What classification code is assigned to this device?
This device is registered under product classification code U0803.
Similar Classification Devices (U0803)
Other Devices by CARESS FLOW Srl
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