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

3D Chest Press Med — Class I MDR by SCHNELL Trainingsgeräte…

MD Atlas
SCHNELL Trainingsgeräte GmbH

EUDAMED last updated this device on Mar 17, 2026

3D Chest Press Med

426254921ANTLMEDK6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SCHNELL Trainingsgeräte GmbH
UDI-DI code: 04262549210012
Reference / catalog number: 1030M

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: SCHNELL Trainingsgeräte GmbH
SRN: DE-MF-000033664
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: 3D Chest Press Med
UDI-DI code: 04262549210012
Basic UDI-DI: 426254921ANTLMEDK6
Reference / catalog number: 1030M
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)

Z120603PASSIVE REHABILITATIVE GYMNASTICS EQUIPMENT

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

3D Seated Row Med426254921ANTLMEDK6On the market 4back Abdominal Med426254921ANTLMEDK6On the market 4back Extension Med426254921ANTLMEDK6On the market 4back Flexion & Extension Med426254921ANTLMEDK6On the market 4back Lateral-Flexion Med426254921ANTLMEDK6On 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.