FDA Device Establishments · JSON-LD · Markdown

Coloplast Manufacturing US, LLC.

FEI 3030087693 · Repack or Relabel Medical Device · Status: Active

FEI Number3030087693
Owner / OperatorColoplast Corp. (#8010144)
Address4008 Heritage Drive, Brookshire, TX, US
Registration expiry2026
Initial importer flagY
Registered products2
Product codes (top 20)FAD, LJE
Regulation § (21 CFR)876.4620
Proprietary namesKolibri Direct Puncture Sets; Kolibri Percutaneous Nephrostomy Kits; Kolibri Percutaneous Nephrostomy Catheters

External sources

Source: openFDA. Public-domain (CC0).