Aqf Limited
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.
ANVISA, brazylijski organ regulacyjny ds. zdrowia, posiada dla tego zakładu ważny certyfikat Dobrej Praktyki Produkcyjnej, obejmujący wyroby medyczne, ważny do 2028-06-08. Certyfikat wydawany jest po inspekcji samego zakładu, dlatego zagraniczny organ regulacyjny nadaje tej witrynie nazwę: towary tu wyprodukowane są dopuszczone do obrotu na rynku brazylijskim. Numer procesu 25351285336202469.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Ireland
- Categories
- Artykuły medyczne i związane z opieką zdrowotną
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 3 official sources are on file. 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
- manufacturing-practice-certified (record type: manufacturing-practice-certified) [official record; status green] A regulator of health products inspected this site and certified how it manufactures the product class named, for example medical devices or cosmetics. It is about manufacturing practice at the site, not a medicines licence. checked 2026-10-17. ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- Listed in a source registry (record type: listed-in-registry) [official record; status amber] Listed in The Companies Registration Office – an Oifig um Chlarú Cuideachtaí; entry number 401268. Matched to this company by name only; no second anchor confirms it is the same legal entity.. Found in a named public register, not only on its own website. checked 2026-08-31. BRIS, EU business registers interconnection (e-justice.europa.eu)
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-09-07. Companies Registration Office (CRO), Ireland
- Annual accounts filed with the register (record type: annual-accounts-filed) [official record; status green] Indicates the company still meets its reporting duties. checked 2026-09-07. Companies Registration Office (CRO), Ireland
- On the company register (record type: registered-since) [official record; status green] Shows how long the company has been on the state register, which is hard to fake and easy to check. checked 2026-09-07. Companies Registration Office (CRO), Ireland
- registry-activity (record type: registry-activity) [official record; status green] Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-09-07. Companies Registration Office (CRO), Ireland
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)