My Dental Laboratory
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.
BENİM Diş Laboratuvarım
MY Dental Lab --> --> MEDİKAL SİSTEM --> Giriş My Dental Lab müşterilere hoş geldiniz! Öncelikle Yönetim Kurulu ve tüm Laboratuvar personeli, geçmiş zamandaki işbirliklerinden dolayı Doktorlara ve Diş Hekimlerine teşekkür eder. Teknisyen becerilerini eğitme ve geliştirmenin yanı sıra, My Dental Lab'in RHM endüstrisindeki restorasyon teknolojisinin gelişimine ayak uydurmasına yardımcı olmak için her zaman en son teknolojiyi güncelliyoruz. Hastaların her zaman en uygun ürünleri kullanmaları için koşullar yaratmak. Hastalara en yüksek faydaları bir araya getirmek için her zaman şirket ve müşteriler arasındaki bağlantıyı ve alışverişi teşvik ediyoruz. Çok teşekkür ederim!
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Ho Chi Minh, Vietnam
- Website
- https://mydental.vn/
- Categories
- Diş Malzemeleri ve Ekipmanları
What is established and what is not
No researcher review has been written for this company yet. No official record 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. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- First recorded on the web archive (record type: web-presence-since) [our own observation, not an official record; status green] The company website was already online in 2021. Shows a web archive saw a page at this address on that date. It does not show who ran the site then. checked 2026-08-04. Internet Archive (Wayback)
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.