FDA Device Establishments · JSON-LD · Markdown
FEI 3015455735 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3015455735 |
|---|---|
| Owner / Operator | Biobeat Technologies LTD (#10082659) |
| Address | 22 Efal st., Petach Tikva Central, 4951122, IL |
| Mandatory US Agent | A. Stein Regulatory Affairs |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 6 |
| Product codes (top 20) | DRG, DQA, DXN, BZQ, DXG, FLL |
| Regulation § (21 CFR) | 870.2910, 870.2700, 870.1130, 868.2375, 870.1435, 880.2910 |
| Proprietary names | BB613WP |
Source: openFDA. Public-domain (CC0).