Pharma Systems Eesti Osaühing
Pharma Systems - Comfort Breathing Every Time
Pharma Systems - Comfort Breathing Every Time Pharma Systems Comfort Breathing Every Time Pharma Systems is a Swedish company that has provided comfort safety breathing systems since 1990. We design, manufacture and deliver a high-quality range of Heat & Moisture Exchangers (HME’s) & Breathing Air Filters with the best features and performance. CONTACT US Advantages with Pharma Systems Heat & Moisture Exchangers (HME’s) & Breathing Air Filters are as follows: Extensive research and development Solid quality system Well documented and tested product design Partnership & Support for our distributors MDD 93/42/EEC - Annex II ISO 13485:2016 / MDSAP EN ISO 13485:2016 Application Areas of our HME’s & Air Filters Anesthesia HME/Filter for anesthesia. Anesthesia enables the painless performance of
- Type
- Manufacturer
- Location
- Riidaküla, Estonia
- Founded
- 1997
- Website
- https://pharmasystems.se/
- Categories
- Tıbbi ve Sağlık Malzemeleri
Listed in a source registry
Verified facts
- ownership-on-record (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-address (green), checked 2026-08-24 e-Äriregister (RIK)
- registered-since (green), checked 1997-11-19 e-Äriregister (RIK)
- directors-on-file (green), checked 2026-08-24 e-Äriregister (RIK)
- leadership-on-record (green), checked 2023-12-11 e-Äriregister (RIK)
- registered-manufacturer (green), checked 2026-08-06 e-Äriregister (teatatud tegevusalad)
- annual-accounts-filed (green), checked 2026-08-07 e-Äriregister (majandusaasta aruanded)
- registry-active-global (green), checked 2026-07-27 e-Äriregister
- debarment-clear (green), checked 2026-07-27 OpenSanctions
- sanctions-clear (green), checked 2026-07-27 OpenSanctions
- tax-filing-active (green), checked 2026-08-15 Estonian Tax and Customs Board, open data on taxes paid
- workforce-on-record (green), checked 2026-08-15 Estonian Tax and Customs Board, open data on taxes paid
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)