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.
マイデンタルラボ
MY Dental Lab --> --> 医療システム --> はじめに My Dental Lab はお客様を歓迎します。まず初めに、理事会とすべての研究所スタッフは、これまでの医師と歯科医師の協力に感謝したいと思います。技術者のスキルのトレーニングと向上に加えて、My Dental Lab が RHM 業界の修復技術の発展に遅れないようにするために、常に最新の技術を更新しています。患者様が常に最適な製品を使用できる状態を作り出すこと。私たちは、患者様に最大の利益をもたらすために、常に企業とお客様とのつながりと交流を促進します。どうもありがとうございます！私たちについて --> コードを入力して保証情報を検索 --> 製品 Rhein 83 接続システム スマート リストア接続システム 詳細を見る K
- 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
- 歯科用品および歯科用機器
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.