gudid Primary ID: 90.2060.113

DCRC 900 Flex ID - Flow Health (UDI 90.2060.113)

Manufactured by Sarstedt Aktiengesellschaft & Co.KG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DCRC 900 Flex ID - Flow Health (Model/Catalog Number: 90.2060.113) is a medical device manufactured by Sarstedt Aktiengesellschaft & Co.KG. This product is indexed under FDA Product Code / Category Classification LXG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 90.2060.113
Product Code / EMDN: LXG
Device Name
Database Sync Date: 2026-08-09 09:46:24

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 DCRC 900 Flex ID - Flow Health?

The registered manufacturer of record for DCRC 900 Flex ID - Flow Health is Sarstedt Aktiengesellschaft & Co.KG.

What is the Primary UDI-DI identifier for DCRC 900 Flex ID - Flow Health?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90.2060.113.

What classification code is assigned to this device?

This device is registered under product classification code LXG.

Similar Classification Devices (LXG)

Other Devices by Sarstedt Aktiengesellschaft & Co.KG

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