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 医学。仪器仪表
我们是该国唯一一家现代化、可靠的医疗和实验室离心机制造商。通过与各个科学、研发中心和实验室的直接合作，我们可以满足客户的要求。
- 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
- 医疗保健用品
- Markets
- 波兰
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 在这里，中标还附带了别人做过的审查：在欧盟和欧洲经济区，公共采购方必须排除因欺诈、腐败或洗钱被定罪的投标人，以及经终局裁决认定拖欠税款或社会保险费的投标人。 这项审查只针对那次招标、截至授标之日：它不说明公司今天的状况，中标也不说明合同已经履行。 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)