Zaklad Produkcji Sprzetu Medycznego RAVIMED Sp. z o.o.
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
Leki
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Lajski, Poland
- Website
- https://ravimed.com.pl
- Categories
- Artykuły medyczne i związane z opieką zdrowotną
- Markets
- Polska
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 6 official records from 5 official sources are on file. 1 other entry is not an official record: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Website domain registered (record type: domain-registered) [our own observation, not an official record; status green] Shows how long this web address has been registered. That is the age of the domain, not of the company: a domain can change owners. checked 2026-08-23. Domain registry record
- EU VAT number valid for cross-border trade (record type: vat-valid) [official record; status green] The number is registered and active: we asked the EU VIES service and it answered yes. An invalid VAT number is the first sign an invoice comes from the wrong company. checked 2026-10-03. Ministry of Finance VAT white list (Poland)
- Street address on file in the state register (record type: registered-address) [official record; status green] Registered address: POLNA 54, 05-119 ŁAJSKI. The address the company itself gave the register, so post and inspectors reach it there. checked 2026-10-03. Ministry of Finance VAT white list (Poland)
- Medicines manufacturing or import authorisation (MIA) (record type: medicines-mia-holder) [official record; status green] A medicines regulator authorises this company to manufacture and/or import medicinal products at the named site. The register lists the authorisation itself, not which products it covers, and it is not a record of trading. effective since 2026-08-15. EudraGMDP manufacturing and importation authorisation register (EMA)
- Line of business as recorded in the state register: PRODUKCJA URZĄDZEŃ, INSTRUMENTÓW ORAZ WYROBÓW MEDYCZNYCH, WŁĄCZAJĄC DENTYSTYCZNE (record type: registry-activity) [official record; status green] Line of business as recorded in the state register: PRODUKCJA URZĄDZEŃ, INSTRUMENTÓW ORAZ WYROBÓW MEDYCZNYCH, WŁĄCZAJĄC DENTYSTYCZNE. Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-10-03. REGON national business register (GUS, Poland)
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-10-03. ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- Takes part in public tenders (record type: public-contract-awarded) [official record; status green] 3 public contracts on record, the latest awarded 2025-08-04. A public buyer selected this supplier through an official tender. Open the source for the contracts themselves. effective since 2025-08-04. TED (Tenders Electronic Daily), EU public procurement award notices Tutaj wygrana niesie też cudzą kontrolę: w UE i EOG zamawiający musi wykluczyć wykonawcę skazanego za oszustwo, korupcję lub pranie pieniędzy oraz takiego, wobec którego prawomocnie stwierdzono zaległości podatkowe lub składkowe. Ta kontrola dotyczyła tamtego postępowania w dniu udzielenia zamówienia: nie pokazuje obecnej sytuacji firmy, a wygrana nie pokazuje, że umowa została wykonana. Directive 2014/24/EU, Article 57 (exclusion grounds)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)