ZHEJIANG VALUE MECHANICAL & ELECTRICAL PRODUCTS CO.,LTD.
VALUE Zhejiang Feiyue Electromechanical Co., Ltd. focuses on the research and development and application of vacuum technology, and is committed to providing customers around the world with comprehensive, high-quality vacuum technology solutions. Its business fields include HVAC engineering, scientific instrument laboratory equipment and medical equipment, semiconductors, food and industry, etc. It uses professional technology to help customers improve efficiency, optimize quality, and help customers succeed.
VALUE Zhejiang Feiyue Electromechanical Co., Ltd. focuses on the research and development and application of vacuum technology, and is committed to providing customers around the world with comprehensive, high-quality vacuum technology solutions. Its business fields include HVAC engineering, scientific instrument laboratory equipment and medical equipment, semiconductors, food and industry, etc. It uses professional technology to help customers improve efficiency, optimize quality, and help customers succeed.
- Type
- Manufacturer
- Location
- Hangzhou, Zhejiang, China
- Website
- valuevacuum.com
- Categories
- Medical & Healthcare Supplies, Pantry & Dry Goods
Listed in a source registry
Verified facts
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- domain-registered (green), checked 2026-08-10 Domain registry record
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)