PhysioFlow (UDI Lab1)

Manufactured by MANATEC

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The PhysioFlow (Model/Catalog Number: Lab1) is a medical device manufactured by MANATEC. This product is indexed under FDA Product Code / Category Classification DSB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Lab1
Product Code / EMDN: DSB
Device Name
Database Sync Date: 2026-08-09 09:33:52

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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Frequently Asked Questions

Who is the primary manufacturer of PhysioFlow?

The registered manufacturer of record for PhysioFlow is MANATEC.

What is the Primary UDI-DI identifier for PhysioFlow?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Lab1.

What classification code is assigned to this device?

This device is registered under product classification code DSB.

Similar Classification Devices (DSB)

Other Devices by MANATEC

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