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

525.00000.7590 — Class I MDR by ERKA Kallmeyer…

MD Atlas
ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

EUDAMED last updated this device on Sep 29, 2025

525.00000.7590

42502961525LS

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft
UDI-DI code: 04250296128919
Reference / catalog number: 525.00000.7590

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: ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft
SRN: DE-MF-000009663
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: 04250296128919
Basic UDI-DI: 42502961525LS
Reference / catalog number: 525.00000.7590
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

C9005PHONENDOSCOPES AND STETHOSCOPES

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

215.24482.729042502961214L6On the market 570.00085.759042502961570LXOn the market 570.00084.759042502961570LXOn the market 570.00055.759042502961570LXOn the market 570.00005.759042502961570LXOn 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.