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.
莫顿医疗
领先一步... Morton Medikal 于 1990 年在伊兹密尔成立，致力于设计和生产人类使用的医疗产品。 Morton Medical 对许多领域的医疗干预和治疗阶段使用的一次性/可重复使用的医疗产品和设备进行产品开发、改进和设计，特别是麻醉、通气和复苏。 Morton Medikal 拥有广泛的产品组和专业制造经验，每年通过开发新产品和型号来增加产品多样性。 Morton Medikal 的生产过程在其新设施的两个不同的 10,000 级和 100,000 级洁净室中进行，并根据 ISO 9001、ISO 13485 和 CE 标准进行管理和监控。
- 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
- 医疗保健用品
- Markets
- 土耳其
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.