Marubun Corporation
Nhà kinh doanh điện tử hướng tới tương lai cung cấp các linh kiện phức tạp và công nghệ cấp không gian
Marubun cung cấp các mô-đun liên lạc vệ tinh, dụng cụ kỹ thuật y tế, lưới định vị hàng không và các dòng chip hoạt động tiêu chuẩn.
- Type
- distributor seeking brands
- Location
- Tokyo, Japan
- Founded
- 1844
- Website
- marubun.co.jp
- Categories
- Điện tử tiêu dùng, Tự động hóa công nghiệp và robot, Vật tư y tế và chăm sóc sức khỏe
- Markets
- Nhật Bản, Trung Quốc, Đài Loan, Singapore, Philippines, Hoa Kỳ, Đức
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- registry-id-verified (green), checked 2026-08-25 gBizINFO (Ministry of Economy, Trade and Industry), government-held corporate data
- named-by-manufacturer (green), checked 2026-09-04 TQ Systems USA Inc distributor list
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- debarment-clear (green), checked 2026-08-09 OpenSanctions
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
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)