MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY
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.
MPW中医学。楽器
当社は、国内で信頼性の高い最新の医療用遠心分離機および実験用遠心分離機を製造する唯一のメーカーです。当社は、さまざまな科学、研究開発センター、研究所との直接協力により、お客様の要件にお応えします。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Warszawa, Poland
- Website
- https://mpw.pl
- Categories
- 医療およびヘルスケア用品
- Markets
- ポーランド
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 4 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: BOREMLOWSKA 46, 04-347 WARSZAWA. 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)
- Registered business units on file (record type: registered-units) [official record; status green] 1 registered business units. The register lists how many sites the company runs. checked 2026-10-03. REGON national business register (GUS, Poland)
- 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] 35 public contracts on record, the latest awarded 2026-09-08. A public buyer selected this supplier through an official tender. Open the source for the contracts themselves. effective since 2026-09-08. TED (Tenders Electronic Daily), EU public procurement award notices ここでの落札は、他者による審査も伴います。EUおよびEEAでは、公共調達者は詐欺、汚職、資金洗浄で有罪となった入札者、および確定した決定で税や社会保険料の未納が認定された入札者を排除しなければなりません。 この審査はその入札の落札日時点のものです。会社の現在の状況を示すものではなく、落札は契約が履行されたことを示すものでもありません。 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)