# WALLAC OY

FEI: 3002808498
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Revvity, Inc. (#9912035)

Address: MUSTIONKATU 6, TURKU Varsinais-Suomi, 20750, FI

Mandatory US Agent: Revvity, Inc.

## Products

Total registered: 1
Top product codes: LOK
Regulation §: —

Proprietary names: AutoDELFIA hAFP kit (B079-212), AutoDELFIA instrument

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002808498%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002808498