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.
مختبر أسناني
مختبر طب الأسنان الخاص بي --> --> النظام الطبي --> مقدمة يرحب مختبر طب الأسنان الخاص بي بالعملاء! في البداية، يود مجلس الإدارة وجميع موظفي المختبر أن يشكروا الأطباء وأطباء الأسنان على تعاونهم خلال الفترة الماضية. بالإضافة إلى التدريب وتحسين مهارات الفنيين، نقوم دائمًا بتحديث أحدث التقنيات لمساعدة My Dental Lab على مواكبة تطور تكنولوجيا الترميم في صناعة RHM. تهيئة الظروف للمرضى لاستخدام أفضل المنتجات دائمًا. نحن نعمل دائمًا على تعزيز الاتصال والتبادل بين الشركة والعملاء لتحقيق أعلى الفوائد للمرضى معًا. شكراً جزيلاً!
- 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
- مستلزمات ومعدات طب الأسنان
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.