FDA Device Establishments · JSON-LD · Markdown

Stryker Sustainability Solutions Phoenix

FEI 3002615969 · Reprocess Single-Use Device · Status: Active

FEI Number3002615969
Owner / OperatorSTRYKER CORP. (#1811755)
Address10232 S. 51st St., Phoenix, AZ, US
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)NLH, DSA
Regulation § (21 CFR)870.1220, 870.2900
Proprietary namesReprocessed EP Catheter and Cable

External sources

Source: openFDA. Public-domain (CC0).