NOTE AB
NOTE AB は、プリント回路基板を製造するスウェーデンの電子機器製造サービス (EMS) 会社です。
NOTE AB はスウェーデンのエレクトロニクス製造サービス (EMS) 会社で、北欧地域の通信、産業、医療、防衛の顧客向けにプリント基板アセンブリ、ボックスビルドエレクトロニクス、組み込みソフトウェア統合を製造しています。スウェーデン、英国、エストニア、中国で工場を運営しているNOTEは、エンジニアリングサポートと連続製造の両方を必要とする中量OEM顧客にサービスを提供しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Norrtälje, Sweden
- Founded
- 1999
- Website
- note.se
- Categories
- 家電, 電気および電力機器, 医療およびヘルスケア用品
- Markets
- スウェーデン, イギリス, フィンランド, ノルウェー, デンマーク, ドイツ
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
- ISO 13485, Medical Devices Quality 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)