RIK LaserMed
치과, 수술, 재활 분야를 위한 의료용 레이저 장비를 생산하는 러시아 제조업체
RIK는 적용 범위를 확장하는 보조 액세서리와 함께 Lasermed-10, L'Med-1 및 L'Med-12 장치를 포함한 의료용 레이저 장비를 생산 및 공급합니다. 응용 분야에는 치과, 외과, 재활 의학이 포함됩니다. 이 회사는 러시아 전역의 진료소 및 의료 시설에 장비를 제공합니다.
- Type
- Manufacturer
- Location
- Russia
- Website
- lasermed.ru
- Categories
- 의료 및 건강 관리 용품, 가전제품
- Markets
- 러시아
Listed in a source registry
Verified facts
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
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)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)