Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

moduflex 2500 — Class IIb MDR by modul technik GmbH

MD Atlas
modul technik GmbH

EUDAMED last updated this device on Jun 25, 2025

moduflex 2500

426241958DVEst3M8

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: modul technik GmbH
UDI-DI code: 04262419580092
Reference / catalog number: moduflex 2500

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: modul technik GmbH
SRN: DE-MF-000014647
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 1, 2016	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262419580092
Basic UDI-DI: 426241958DVEst3M8
Reference / catalog number: moduflex 2500
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120309MEDICAL/MEDICINAL GAS PIPELINE SYSTEMS AND RELATED ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

ambient compact426241958modul8GDOn the market ambient cube426241958modul8GDOn the market ambient junior426241958modul8GDOn the market ambient light426241958modul8GDOn the market ambient simplex426241958modul8GDOn the market

Certificates

Certificate health across this manufacturer's portfolio.

44911222228Issued
Quality management systemNotified body: 0044Expiry: Dec 2, 2030