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

WindEze — Class IIa MDD by Merckle GmbH

MD Atlas
Merckle GmbH

EUDAMED last updated this device on Oct 31, 2025

WindEze

B-314958PH

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Merckle GmbH
UDI-DI code: D-314958PH
Reference / catalog number: 314958

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: Merckle GmbH
SRN: DE-MF-000018230
Manufacturer status: Active

Critical warnings

6 warnings recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.
CW277
EUDAMED did not publish a description for this code.
CW999
Do not take Wind-eze Gel Caps: if you are allergic to simeticone or any of the other ingredients.
CW999
Do not take Wind-eze Gel Caps: if you are under 12 years
CW999
If symptoms persist for more than 14 days, or if symptoms worsen, medical advice must be sought.
CW999
Not recommended for children under 12 years.

Market distribution

Primary placement in Ireland; available across 1 country total.

Country	On market since	Until
IrelandPrimary placement	Feb 27, 2019	Still on market

Device identification

Trade name: WindEze
UDI-DI code: D-314958PH
Basic UDI-DI: B-314958PH
Reference / catalog number: 314958
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC 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)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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

InfacolB-307356NROn the market Macragol PowderB-251267NROn the market MonasensB-237677Q4On the market Naso-NaCl (ampoules, eyes, nose)B-146289PEOn the market NebuMarB-269955RQOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.