Sale on Ophthalmic Equipment - Starting from 16 November!
Hospital companies, practices and trauma centres across Austria can ask us for documented quotes on certified medical equipment and supplies. Send the model or the specification, and the quote will cover the German or English documents your team needs, the MPBV acceptance test and the route by rail, road or air into Austria.
Austria has no coastline, so a crate from an overseas factory is usually cleared at a major EU entry point abroad and finishes its trip by rail or road. Smaller items can fly straight into Vienna, Linz or Graz. Long before that, though, an order has to clear two hurdles: can the device be supplied under Austria's Medical Devices Act of 2021, and who in the chain holds which registration?
We're MediGear, and we are registered in England and Wales as a medical equipment distributor. Our team quotes, documents and ships certified equipment for healthcare buyers in more than 80 countries. Send the requirement, and we start looking for verified makers who can supply it, along with the points an Austrian site will ask about. You get back a quote your clinical and purchasing teams can work with. Requests go through our buyers page, and nobody needs an account.
Requests reach us from public, non-profit and private providers across healthcare in Austria:
They buy in very different ways. Publicly owned hospitals in Austria can buy through Bundesbeschaffung GmbH, the federal central buyer. Its tenders follow the 2018 procurement law and run on the ANKÖ-Vergabeportal, where e-procurement is now mandatory. A dental practice in Tyrol replacing one X-ray machine, by contrast, wants a straight quote and a date. We first determine what kind of purchase it is, because that decides what the quote must include.
Alongside the EU Medical Devices Regulation, Austria has its own Medical Devices Act of 2021. The Austrian Federal Office for Safety in Health Care (BASG) is the authority for medical devices. The act sets the language rule: information supplied with a device must be in German, and English is allowed only for devices reserved for professional users. BASG's guidance for importers points to Articles 13 and 14 of the MDR, which set out the checks importers and distributors make before supplying a device.
Under the MDR, an importer has to be established in the EU. So who holds that role when a hospital brings a unit in from the UK or Asia is for the hospital and its own advisers to settle; EUDAMED registration of economic operators has been mandatory since May 2026. An Austrian distributor also registers with Gesundheit Österreich GmbH before it starts trading. We hold no Austrian importer or distributor registration, and we cannot give regulatory advice. Every quote states the unit's certification, so your team can check it against the medical device regulations in Austria.
Radiation work comes under the Radiation Protection Act of 2020, and every activity needs a licence before it starts. For medical and veterinary X-ray, the licensing authority is the governor of each federal state, as the health ministry explains in its notes on licensing in medicine. Where a room needs structural shielding, the process runs in two stages: a construction licence, then an operating licence.
The authority then inspects an X-ray installation every three years, or every four years for dental and veterinary units. Under the medical radiation protection rules, an acceptance test is needed before first clinical use, and again if a unit has stood unused for more than two years. A supply firm may carry out that test for the products it sells. Speak to your state office while the quote is still open, and we will send the technical data it asks for.
A sound quote rests on a sound specification, so these are the checks we run with the maker for Austrian sites:
We would rather ask the maker a question before quoting than see a medical imaging system held up at commissioning.
For goods from outside the EU, the customs office works from an electronic declaration and its supporting documents, so each order leaves with:
Wood is checked here. The Federal Office of Forests says the import checks on wood packaging from risk countries follow an EU regulation from January 2024. ISPM 15 crates must be debarked, treated and marked, and heat treatment means holding the core at 56 degrees Celsius for at least 30 minutes, though other approved treatments exist. We ask for treated, clearly stamped crates from the start rather than risk a hold at the border.
Delivery is to the port, terminal or airport you nominate. From there it is your import: the declarant or a representative files the electronic customs declaration with Zollamt Österreich, and you arrange the last leg to site. From 1 November to 15 April, lorries over 3.5 tonnes need winter tyres, which is worth knowing for Alpine routes. Devices shipped from inside the EU cross no customs border.
You can order a single unit on most catalogue lines, which suits a practice replacing one monitor or one autoclave. We also quote multi-line requests, such as a new ward for a provincial hospital; for a lab build, see laboratory setup. Laboratory equipment suppliers can also send us a build list, and we will quote it line by line. Theatre and reprocessing teams can browse Sterilisation and Disinfection. Our refurbished range covers pre-owned units too, and Austrian law applies its operating rules to devices that are made available again. A refurbished X-ray unit needs its acceptance test before first clinical use, just as a new one does.
The information on this page is general and meant for buyers in Austria. We make no offer to supply through it, and nothing here is legal, regulatory or customs advice. Quotes are subject to what makers can supply, and no order is binding until both sides confirm it in writing. Whether a device can be supplied in Austria depends on its CE status, intended use, and the language rules of the Medical Devices Act, and X-ray equipment requires a separate licence under the Radiation Protection Act from the state authority. Clearing the goods and checking the regulatory status of your purchase are your responsibility. We act in Austria neither as an importer nor as a registered distributor.
Which hospital or practice is the unit for, and what does it replace? A model number, a data sheet or a photo is enough, and our reply is a quote covering German labelling, the acceptance test papers and the route into Austria.
An account isn't required. Send the model or specification by email to connect@medigear.uk or through the RFQ form on the buyer's page. We quote for state hospital companies, university hospitals, AUVA sites, private groups, dental and veterinary practices and distributors.
Yes, as a rule. The Medical Devices Act requires the information supplied with medical devices in Austria to be in German, while devices reserved for professional users may come with English information. We check what the manufacturer supplies before we quote and flag any gap.
Under the MDR, the importer must be established in the EU and registered in EUDAMED, so who holds that role when an Austrian hospital imports from the UK is for the hospital and its advisers to determine. Distributors based in Austria register with Gesundheit Österreich GmbH before trading. Check your own position with BASG or an adviser before ordering.
The governor of each federal state licenses medical and veterinary X-ray under the Radiation Protection Act. Rooms that need structural shielding require a construction licence, and then an operating licence, and the authority inspects them every three years, or every four years for dental and veterinary units.
Sea freight lands at a large EU port and travels on by rail or road, and air freight can fly into Vienna, Linz or Graz. Delivery is to the port, terminal or airport you nominate, and the last leg to your hospital or practice is your responsibility.
You do, normally through a declarant or representative who files the electronic declaration with Zollamt Österreich. We provide the commercial invoice, packing list, certificate of origin, HS codes,s and CE documents. A unit that comes from inside the EU needs no customs clearance.
Yes. On most catalogue lines, a single unit is fine, from a monitor to a portable X-ray machine, and we mention any minimum order quantity as soon as a maker sets one. Tell us about the final road too, whether that is a pass in winter or a narrow access, and we will ask for packing to suit.
The maker's stock matters most, along with whether the unit is new or refurbished, where it ships from and whether it comes by sea and rail, by road or by air. You will find the lead time and route on the quote, and email updates follow from dispatch until it arrives.