Semikal Teknoloji Sanayi ve Ticaret Anonim Sirketi
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.
Semical Biosurgery - Semical is a regenerative medicine company that has conducted research and deve
Skip to the content New horizons for medical solutions VIEW more *The leader of next-generation biomaterials, Semical offers the health solutions of the future. 01 Op Orthopedics *Category Products 02 B Bioresorbable *Category Products 03 Ma Medical Aesthetic *Category Products 04 Sc Skin Care *Category Products *With advanced R&D and production infrastructure, Semical is shaping the future today. Semical is a regenerative medicine company that places science and innovation at the center. The company develops innovative and innovative products with over 25 years of research and development activities by its R&D team, and produces various pharmaceutical forms according to the needs of the industry.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Isparta, Turkey
- Website
- https://semical.com.tr
- Categories
- Suprimentos médicos e de saúde
- Markets
- Turquia
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. 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
- 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.