Morton Medikal San. ve Tic. A.S.
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.
모튼 메디컬
한 발 앞서... Morton Medikal은 1990년 이즈미르에서 설립되어 인체용 의료 제품을 설계하고 생산했습니다. Morton Medical은 특히 마취, 환기 및 재활성화 등 여러 분야의 의료 개입 및 치료 단계에 사용되는 일회용/재사용 의료 제품 및 장비에 대한 제품 개발, 개선 및 설계를 수행합니다. 전문적인 경험을 바탕으로 제조된 폭넓은 제품군을 보유하고 있는 Morton Medikal은 매년 새로운 제품과 모델을 개발하여 제품의 다양성을 높이고 있습니다. 새로운 시설에 있는 10,000등급과 100,000등급의 두 가지 클린룸에서 생산 공정을 수행하는 Morton Medikal은 ISO 9001, ISO 13485 및 CE 표준에 따라 관리 및 모니터링됩니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Izmir, Turkey
- Website
- https://mortonmedical.net
- Categories
- 의료 및 건강 관리 용품
- Markets
- 튀르키예
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 1 official record from 1 official source is 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
- 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
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)
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.