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

Bretex Kubi Med I 14 310 090/200 — Class I MDR

MD Atlas
Breckle Matratzenwerk Weida

EUDAMED last updated this device on Feb 16, 2026

Bretex Kubi Med I 14 310 090/200

40194730024F

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Breckle Matratzenwerk Weida
UDI-DI code: 04019473595223
Reference / catalog number: Bretex Kubi Med I 14 310 090/200

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: Breckle Matratzenwerk Weida
SRN: DE-MF-000010222
Manufacturer status: Active

Related devices

Aqua12 302 090/20040194730024FOn the market Aqua12 302 087/20840194730024FOn the market Aqua12 302 087/20040194730024FOn the market Aqua12 304 100/20040194730024FOn the market Aqua12 304 090/20040194730024FOn 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.

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: 04019473595223
Basic UDI-DI: 40194730024F
Reference / catalog number: Bretex Kubi Med I 14 310 090/200
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: Medical mattress with hygienic cover
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

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