FLAIR WRITING EQUIPMENTS PRIVATE LIMITED
- Type
- Manufacturer
- Location
- Dungari Gujarat, India
- Categories
- Dental Supplies & Equipment
Listed in a source registry
Verified facts
- market-access-us (green), checked 2026-08-23 FDA device establishment registration (openFDA, U.S. Food and Drug Administration)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- registry-id-verified (green), checked 2026-07-15 MCA21, Ministry of Corporate Affairs
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)