Sale on Ophthalmic Equipment - Starting from 16 November!
Israel's medical equipment register relies on approvals from recognised countries, such as FDA and CE, so our quotes start from the certificates a model already holds. Send the model or specification, and we will set out those papers, the radiation licensing steps and sea freight to the Mediterranean port you nominate.
Medical devices are listed on the Medical Equipment Register, which AMAR, the medical device division of the Ministry of Health, maintains. A device gets on the register through approvals it already has from recognised countries, such as the FDA and CE. The Israeli registration holder then takes responsibility for quality, the supply chain, and the import itself. CT and MRI in Israel add one more step, since the hospital needs a licence from the Director General before it acquires one.
We're MediGear. As a medical equipment distributor with our company registered in England and Wales, we work for healthcare buyers in more than 80 countries on quotes, documents, and freight. Please tell us the model you have in mind, or the clinical need, whether it is for imaging and advanced diagnostics in Israel or for ward monitors, and we then look for verified manufacturers whose models already hold approvals that Israel accepts. Your engineers and buying staff get a quote that covers the points below. Send requests through our buyers page, and there's no account to set up.
Healthcare in Israel rests on universal insurance: every resident is insured under the State Health Insurance Law and signs up with a health fund. Our quotes go to providers of health care in Tel Aviv, Haifa and the south, and to those who supply them:
Government tenders, central tenders and exemption notices are posted on the Government Procurement Administration's website. A dental clinic that needs one new panoramic unit needs a clear quote and a registration holder for the model.
AMAR runs the register under the Medical Equipment Law of 2012 and rules made in 2013. Applications are submitted electronically, through its vault system. Since 1 January 2025, the registration procedure lists the required documents, and the device's full name must be provided in Hebrew and English. Class I devices from recognised countries can use a quick declaration route, renewed each year, and Class II, IIa and IIb devices have a fast track. Translated documents need a translator's verification.
A registration lasts as long as the foreign certificates behind it. The Ministry accepts old EU certificates that EU rules have extended, up to 31 December 2027 or 2028 by class. Under its 2023 reform plan, AMAR approval also serves as import approval. The holder carries quality, the supply chain and the import, a role we cannot take, and this page is not regulatory advice.
Holding a medical radiation device requires a Ministry of Health licence, issued by its radiation devices licensing unit and automatically renewed each January. The device must be AMAR-approved. No unit may go in before the licensing unit approves the room plans, and rooms are designed so that yearly doses stay under 2 mSv for staff and 0.3 mSv for the public. Computed tomography, MRI, PET, cath-lab and angio systems also need the Director General's written licence before they are acquired.
Once a unit is in, Ministry inspectors test radiation safety and image quality on diagnostic units, and then the licence takes effect. Later checks come as often as the unit's director decides. Users follow the maker's quality control routine, and sites running mammography equipment test with an ACR phantom every week. A certified radiographer runs the equipment, except for some dental imaging and bone density scans, and medical imaging institutes are advised to involve a medical physicist, including for acceptance tests. Changes must be reported within 15 days, and replacing equipment in an existing room counts as a new installation.
Our questions for the manufacturer before the order:
Open points go to the maker in writing before we quote. The Ministry's post-installation check looks at both safety and image quality, so the papers need to be right.
Israeli customs needs the details of foreign suppliers listed in its Shaar Olami system before importers can file their declarations. The AMAR approval is checked at import through the Maslul system. Every order goes out with these papers:
Israel's plant health body is PPIS, the Plant Protection and Inspection Services of the Ministry of Agriculture. We found no Israeli guidance on wood packing, so we ask makers for crates marked to ISPM 15.
At the port or airport, your customs agent clears the goods with Israeli customs, and the last leg to the hospital is yours. Shipping conditions can change at short notice, so we confirm the route when you order.
A single monitor for a clinic in Haifa is quoted the same way as a full ward, on most catalogue lines. Larger projects can follow the private tender route, and ward teams can browse Hospital Furniture and Fixtures. Teams weighing several imaging systems can list each model in one request. Pre-owned units are part of our refurbished range. For X-ray machines in Israel, the Ministry's rules accept used units within age limits: up to 8 years for a CR unit and 12 for a DR unit, with exceptions on request. A used CT or MRI system still needs the Director General's licence, since the rule covers any transfer. Every unit must also be AMAR-approved.
This is general information for Israeli hospitals and clinics. It makes no offer of supply, and legal, regulatory or customs questions require independent advice. What we quote depends on the maker's supply, and only a written agreement from both sides makes an order. Devices need AMAR approval, and radiation devices need a Ministry of Health licence before use. Clearance and the regulatory side sit with the registration holder and your importer, as we are neither.
CT systems and MRI, PET and cath-lab units need the Director General's written licence before they are acquired. Tell us the model and the hospital, and the quote will list the certificates, the age of any used unit and the sailing.
Public hospitals, health funds, private networks, dental clinics and registration holders can all write to connect@medigear.uk or use the RFQ form on the buyers page, without opening an account. A model number or a specification is enough to begin, whether it comes from a Tel Aviv health care provider or a clinic elsewhere, and replies come by email.
Devices are entered in the Medical Equipment Register kept by AMAR, and every licensed radiation device must be AMAR-approved. Registration relies on approvals from recognised countries, such as FDA and CE, and it lasts only while those certificates are valid.
The party that holds the registration in Israel and, under the Ministry's 2023 reform outline, is responsible for product quality, the supply chain and the actual import. We are not a registration holder, so the maker's Israeli partner or your distributor takes that role.
After installation, the room plans must be approved first. Once the unit is in, Ministry inspectors check radiation safety and image quality on diagnostic devices before the licence takes effect. Later inspections follow at a frequency set by the licensing unit's director.
We can quote the route to Haifa, Ashdod or another Mediterranean port you nominate, and smaller items can fly into Ben Gurion Airport. We confirm the route when the order is placed, and your agent handles clearance and the last leg from the port.
Israeli customs needs the details of foreign suppliers listed in its Shaar Olami system before importers file their declarations. With each consignment of medical equipment and supplies, we send the invoice, packing list, origin papers, HS codes and the model's certificates.
Yes. One unit is fine on most catalogue lines, and if the maker sets a minimum order, the first reply mentions it. A periapical or panoramic unit for a clinic's own patients needs no structural plan, but a dental CT does.
Under the Ministry's licensing guidelines, a used CR unit may be up to 8 years old and a used DR unit up to 12, and exceptions can be requested in special cases. Please tell us the age you need, and the quote will state the unit's date of manufacture.