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.
我的牙科实验室 --> --> 医疗系统 --> 简介 我的牙科实验室欢迎客户！首先，董事会和所有实验室工作人员要感谢医生和牙医过去一段时间的合作。除了培训和提高技术人员技能外，我们始终更新最新技术，帮助 My Dental Lab 跟上 RHM…
我的牙科实验室 --> --> 医疗系统 --> 简介 我的牙科实验室欢迎客户！首先，董事会和所有实验室工作人员要感谢医生和牙医过去一段时间的合作。除了培训和提高技术人员技能外，我们始终更新最新技术，帮助 My Dental Lab 跟上 RHM 行业修复技术的发展。为患者创造条件，始终使用最优化的产品。我们始终促进公司与客户之间的联系和交流，共同为患者带来最高的利益。非常感谢！关于我们 --> 输入代码查询保修信息 --> 产品 Rhein 83 连接系统 智能修复连接系统 查看详情 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
- 牙科用品和设备
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.