# Coloplast Manufacturing US, LLC.

FEI: 3030087693
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: Coloplast Corp. (#8010144)

Address: 4008 Heritage Drive, Brookshire, TX, US



## Products

Total registered: 2
Top product codes: FAD, LJE
Regulation §: 876.4620

Proprietary names: Kolibri Direct Puncture Sets, Kolibri Percutaneous Nephrostomy Kits, Kolibri Percutaneous Nephrostomy Catheters

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223030087693%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3030087693