Medical Precision B.V.
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.
Medical Precision
Trang chủ - Medical Precision Chúng tôi tập trung vào việc cải thiện hành trình của bệnh nhân! Comfort Marker 2.0 mang lại mức độ thoải mái mới khi bắt đầu điều trị cho bệnh nhân. Sản phẩm của chúng tôi Comfort Marker 2.0. Cải thiện hành trình xạ trị của bệnh nhân và đạt được hiệu quả lâm sàng với Comfort Marker 2.0, được phát triển bởi Medical Precision B.V. Thiết bị điểm tham chiếu mang tính cách mạng này mang lại mức độ thoải mái mới khi bắt đầu điều trị bằng xạ trị cho bệnh nhân. Hệ thống dễ sử dụng này được thiết kế đặc biệt để sử dụng trong xạ trị bằng công nghệ phổ biến trong ngành trang điểm vĩnh viễn. Thiết bị này được thiết kế cẩn thận để áp dụng các dấu tham chiếu bằng cách tiêm độ sâu có kiểm soát, giúp bệnh nhân ít đau hơn so với các phương pháp đánh dấu khác.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Zwolle, Netherlands
- Website
- https://medicalprecision.nl
- Categories
- Vật tư y tế và chăm sóc sức khỏe
- Markets
- Hà Lan
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 2 official records from 2 official sources are on file. 4 other entries are not official records: 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. 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
- Business email on the company's own domain (record type: corporate-mail-on-domain) [our own observation, not an official record; status green] Shows the domain runs its own email rather than a free mailbox. It describes the domain, not who owns it. checked 2026-08-22. Mail server of the company domain
- Website domain registered (record type: domain-registered) [our own observation, not an official record; status green] Shows how long this web address has been registered. That is the age of the domain, not of the company: a domain can change owners. checked 2026-08-22. Domain registry record
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-22. OpenSanctions
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-22. OpenSanctions
- Legal entity ID lapsed (record type: lei-lapsed) [official record; status amber] The global finance identifier was not renewed. checked 2026-08-22. GLEIF
- 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)