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

Sensigo — Class IIa MDR by Synthon Hispania S.L.

MD Atlas
Synthon Hispania S.L.

EUDAMED last updated this device on Mar 10, 2026

Sensigo

8434283-MD.aid.001-DX

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Synthon Hispania S.L.
UDI-DI code: 08434283000228
Reference / catalog number: Sensigo

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: Synthon Hispania S.L.
SRN: ES-MF-000004771
Manufacturer status: Active

Related devices

Autoxon8434283-MD.aid.001-DXOn the market Autoxon8434283-MD.aid.001-DXOn the market Autoxon8434283-MD.aid.001-DXOn the market Autoxon8434283-MD.aid.001-DXOn the market Myject8434283-MD.aid.001-DXOn 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.

Market distribution

Primary placement in Austria; available across 1 country total.

Country	On market since	Until
AustriaPrimary placement	Feb 27, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08434283000228
Basic UDI-DI: 8434283-MD.aid.001-DX
Reference / catalog number: Sensigo
Issuing entity: GS1

Classification

Risk category: Class IIa
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)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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