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

91110100 — Class I MDR by flow-med GmbH

MD Atlas
flow-med GmbH

EUDAMED last updated this device on Dec 22, 2025

91110100

4260277010096V

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: flow-med GmbH
UDI-DI code: 04260277012175
Reference / catalog number: 91110100

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: flow-med GmbH
SRN: DE-MF-000006336
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
ULTRAVIOLET LIGHT - DO NOT LOOK DIRECTLY INTO LIGHT !

Market distribution

Primary placement in Netherlands; available across 1 country total.

Placed on the market in Netherlands; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04260277012175
Basic UDI-DI: 4260277010096V
Reference / catalog number: 91110100
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Electronic drying cap for all hearing aids. Global-version, white/anthracite incl. universal USB power supply, 2xUSB-C cable, Adapter EU, US, UK, AUS, Instruction for use
Additional information URL: https://downloads.flow-med.com/user_guide_dry-cap_uv22.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y214580HEARING AIDS OR HEARING DEVICES - 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

905101004260277010046KOn the market 910101004260277010096VOn the market 912101004260277010096VOn the market 704202014260277010026FOn the market 913101004260277010046KOn 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.