# MERIDIAN AG

FEI: 3003282815
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: MERIDIAN AG (#8030988)

Address: BIERIGUTSTRASSE 7, THUN Bern, CH-3608, CH

Mandatory US Agent: Regulatory Insight, Inc.

## Products

Total registered: 1
Top product codes: HQF
Regulation §: 886.4390

Proprietary names: MR Q, MR Q Supine, MR Q SLT

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003282815%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003282815