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

Y-Adapter - shock spoon holder — Class I MDR

MD Atlas
GS Elektromedizinische Geräte G. Stemple GmbH

EUDAMED last updated this device on Jan 8, 2026

Y-Adapter - shock spoon holder

42601783500019JE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GS Elektromedizinische Geräte G. Stemple GmbH
UDI-DI code: 04260178357870
Reference / catalog number: 04327.6

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: GS Elektromedizinische Geräte G. Stemple GmbH
SRN: DE-MF-000007648
Manufacturer status: Active

Critical warnings

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

CW018
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: Y-Adapter - shock spoon holder
UDI-DI code: 04260178357870
Basic UDI-DI: 42601783500019JE
Reference / catalog number: 04327.6
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: https://www.corpuls.world/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12030580DEFIBRILLATORS - HARDWARE ACCESSORIES

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

4-pole M-ECG-cable c3/c1 2.0m f. neonates/infants42601783500002HVOn the market 4-pole M-ECG-cable c3/c1 2.0m with clips/AHA42601783500002HVOn the market 4-pole M-ECG-cable c3/c1 2.0m with clips/ERC42601783500002HVOn the market 4-pole M-ECG-cable c3/c1 2.0m with clips/ERC42601783500002HVOn the market 4-pole M-ECG-cable c3/c1 2.0m with snaps/ERC42601783500002HVOn 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.