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

4262376810232 — Class I MDR by 5MED GmbH

MD Atlas
5MED GmbH

EUDAMED last updated this device on Dec 18, 2025

4262376810232

426237681sippahomev1KU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: 5MED GmbH
UDI-DI code: 04262376810232
Reference / catalog number: 4262376810232

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: 5MED GmbH
SRN: DE-MF-000027746
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04262376810232
Basic UDI-DI: 426237681sippahomev1KU
Reference / catalog number: 4262376810232
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: sippa home is a drinking aid for individuals with swallowing disorders (dysphagia) or aspiration risks. It enables drinking in a safe, head-forward position (chin-tuck maneuver) and is suitable for people with limited head, neck, or arm mobility.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y150915GLASSES AND CUPS

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

4262376810225426237681sippahomev1KUOn the market 4262376810218426237681sippahomev1KUOn the market 4262376810249426237681sippahomev1KUOn the market 4262376810256426237681sippahomev1KUOn 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.