# ALLERGAN

FEI: 3006108784
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: AbbVie, Inc. (#2011068)

Address: 900 PARKWAY GLOBAL PARK, LA AURORA DE HEREDIA, 191-3006, CR

Mandatory US Agent: ABBVIE, INC.

## Products

Total registered: 1
Top product codes: KDD
Regulation §: 878.4800

Proprietary names: Insertion Sleeve; Keller Funnel; Keller Funnel 2, Fill Tube Kit

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006108784%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006108784