FDA Device Establishments · JSON-LD · Markdown
FEI 3008177921 · Develop Specifications But Do Not Manufacture At This Facility Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3008177921 |
|---|---|
| Owner / Operator | SAFERSONIC Medizinprodukte Handelsges.m.b.H (#10057303) |
| Address | Hauptstrasse 16/2, Persenbeug Niederosterreich, A-3680, AT |
| Mandatory US Agent | Regulatory Insight, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ITX |
| Regulation § (21 CFR) | 892.1570 |
| Proprietary names | S11103 Pajunk Labeled Safersonic Single; S11104 Pajunk Labeled Safersonic Conti; DAN-33812 Safersonic Conti; DAN-33825 Safersonic Long; DAN-33812U Safersonic Conti Non Sterile; DAN-33803 Safersonic Single; DAN-33803U Safersonic Single Non Sterile; DAN-33805 Safersonic Medium; DAN-33805U Safersonic Medium Non Sterile; DAN-33803NT Safersonic Single - No Tape |
Source: openFDA. Public-domain (CC0).