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

VE00049 — Class I MDR by Anton Hübner GmbH & Co.…

MD Atlas
Anton Hübner GmbH & Co. KG

EUDAMED last updated this device on Sep 22, 2025

VE00049

4010160GMDN4533263

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Anton Hübner GmbH & Co. KG
UDI-DI code: 04010160003687
Reference / catalog number: VE00049

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: Anton Hübner GmbH & Co. KG
SRN: DE-MF-000006418
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 3 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market
Poland		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04010160003687
Basic UDI-DI: 4010160GMDN4533263
Reference / catalog number: VE00049
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: Pumpdosieraufsatz/Provokations-Test
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A030499ADMINISTRATION KITS - 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

ACTIVOX Compressed lozengeB-DE-MF-000006418-AHVHOn the market ACTIVOX SPRAY NASALB-03578835505160On the market ACTIVOX® Spray NasalB-08715345006199On the market ARKOTOS SyrupB-DE-MF-000006418FEOn the market VI00872B-05600372741737On 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.