# ZIEMER OPHTHALMIC SYSTEMS AG

FEI: 3004858034
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: ZIEMER OPHTHALMIC SYSTEMS AG (#9067737)

Address: ALLMENDSTRASSE 11, PORT Bern, CH - 2562, CH

Mandatory US Agent: Regulatory Insight, Inc.

## Products

Total registered: 2
Top product codes: GEX, HNO
Regulation §: 878.4810, 886.4370

Proprietary names: Procedure Packs LCS, Intershield for LCS, FEMTO Crystal Line, Procedure Packs

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004858034%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004858034