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

ZEISS Mobile Centration — Class I MDR by Carl Zeiss Vision GmbH

MD Atlas
Carl Zeiss Vision GmbH

EUDAMED last updated this device on Jan 12, 2026

ZEISS Mobile Centration

42506686-S01-ZMC-3M

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Carl Zeiss Vision GmbH
UDI-DI code: 04250668607233
Reference / catalog number: 00000-2750-321

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: Carl Zeiss Vision GmbH
SRN: DE-MF-000006173
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: ZEISS Mobile Centration
UDI-DI code: 04250668607233
Basic UDI-DI: 42506686-S01-ZMC-3M
Reference / catalog number: 00000-2750-321
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: http://www.zeiss.com/IFU
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q0299OPHTHALMIC DEVICES - OTHER

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

i.Terminal 242506686-S01-IT2-XEOn the market i.Terminal 2 Station42506686-B01-IT2S-UROn the market i.Terminal go42506686-S01-ITGO-BTOn the market i.Terminal mobile42506686-S01-ITM-ZUOn the market VISUCONSULT 50042506686-S02-VC500-JTOn 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.