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

7067-9-8050_V024 — Class IIb MDD by PROTEC X-ray Systems GmbH

MD Atlas
PROTEC X-ray Systems GmbH

EUDAMED last updated this device on May 6, 2026

7067-9-8050_V024

B-04260502643013

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: PROTEC X-ray Systems GmbH
UDI-DI code: 04260502643013
Reference / catalog number: 7067-9-8050_V024

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: PROTEC X-ray Systems GmbH
SRN: DE-MF-000048351
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260502643013
Basic UDI-DI: B-04260502643013
Reference / catalog number: 7067-9-8050_V024
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://www.protec-med.com/download
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11039005RADIOGENIC COMPLEXES

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

7051-9-5120426050264X018ZUOn the market 7051-9-3125426050264X018ZUOn the market 7051-9-1125426050264X018ZUOn the market 7051-9-1120426050264X018ZUOn the market 7051-9-5121426050264X018ZUOn 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.