Revvity
診断薬、ライフサイエンス試薬および分析機器。
Revvity は、ウォルサムの事業から診断薬、ライフサイエンス試薬、分析機器を製造しています。同社は、上場主要市場全体でヘルスケア システム、研究所、OEM パートナー、または規制対象の輸出顧客に供給しています。
- Type
- Manufacturer
- Location
- Waltham, United States
- Founded
- 1937
- Website
- revvity.com
- Categories
- 医療およびヘルスケア用品, 産業機械
- Markets
- アメリカ合衆国, ドイツ, 日本, シンガポール
Verified facts
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- fda-registered (green), checked 2026-08-12 FDA
- domain-registered (green), checked 2026-08-14 Domain registry record
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- ISO 9001, Quality Management IAF CertSearch
- FDA Registered FDA Establishment Registration
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)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission