GUDIDData
eudamed_udi Primary ID: 08057760160002

Caress Flow (UDI 08057760160002)

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 - Primary ID 08057760160002

Device Regulatory Overview

The Caress Flow (Model/Catalog Number: Caress Flow) is a medical device manufactured by CARESS FLOW Srl. This product is indexed under FDA Product Code / Category Classification Z120899 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Caress Flow
Product Code / EMDN
Z120899
Device Name
Caress Flow
Database Sync Date
2026-08-09 16:46:08

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Caress Flow?

The registered manufacturer of record for Caress Flow is CARESS FLOW Srl.

What is the Primary UDI-DI identifier for Caress Flow?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057760160002.

What classification code is assigned to this device?

This device is registered under product classification code Z120899.

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