GORAN PHARMA PVT. LTD.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Sihor Gujarat, India
- Founded
- 1992
- Categories
- Tandheelkundige benodigdheden en apparatuur
Listed in a source registry
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
- registered-address (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- market-access-us (green), checked 2026-08-23 FDA device establishment registration (openFDA, U.S. Food and Drug Administration)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registered-since (green), effective since 1992-02-07 Company Master Data (Ministry of Corporate Affairs)
- registry-activity (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- registry-id-verified (green), effective since 2026-07-15 MCA21, Ministry of Corporate Affairs
Claimed certifications, not confirmed by us
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
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)