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

SENNEX — Class IIb MDD by Bionmed Technologies GmbH

MD Atlas
Bionmed Technologies GmbH

EUDAMED last updated this device on Apr 23, 2026

SENNEX

B-04262421840009

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Bionmed Technologies GmbH
UDI-DI code: 04262421840009
Reference / catalog number: 70100

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: Bionmed Technologies GmbH
SRN: DE-MF-000005347
Manufacturer status: Active

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW273
EUDAMED did not publish a description for this code.
CW015
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	May 12, 2013	Still on market
Sweden	Feb 5, 2014	Still on market

Device identification

Trade name: SENNEX
UDI-DI code: 04262421840009
Basic UDI-DI: B-04262421840009
Reference / catalog number: 70100
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: SENNEX® Tumor System mit EPT/ECT (Elektroporation-/Elektrochemotherapie) dient zur Behandlung von kutanen und subkutanen Tumoren, sowie Metastasen, in denjenigen Fällen, in denen eine palliative Behandlung sinnvoll ist. Die Tumore werden von der Hautoberfläche her über minimal invasive Nadelelektroden behandelt.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

BionMed clinical (Model: LipusPlus)42624218410100HEOn the market 1010042624218410100HEOn 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.