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

90-02-1050 — Class I MDR by GETSCH+HILLER…

MD Atlas
GETSCH+HILLER Medizintechnik GmbH

EUDAMED last updated this device on Apr 8, 2026

90-02-1050

4059426CONT2N

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GETSCH+HILLER Medizintechnik GmbH
UDI-DI code: 04059426241067
Reference / catalog number: 90-02-1050

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: GETSCH+HILLER Medizintechnik GmbH
SRN: DE-MF-000007007
Manufacturer status: Active

Related devices

30-30129.45AB-04059426153285On the market 90-02-10014059426CONT2NOn the market 90-02-10014059426CONT2NOn the market 90-02-1101-504059426CONT2NOn the market 90-02-1101-044059426CONT2NOn 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.

Country	On market since	Until
GermanyPrimary placement	Apr 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04059426241067
Basic UDI-DI: 4059426CONT2N
Reference / catalog number: 90-02-1050
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: 1/1 Siebkorb, Boden
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

S010401TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS

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