FDA Device Establishments · JSON-LD · Markdown
FEI 3003610251 · Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device · Status: Active
| FEI Number | 3003610251 |
|---|---|
| Owner / Operator | DREVE OTOPLASTIK GMBH (#9028387) |
| Address | MAX-PLANCK-STR. 31, UNNA North Rhine-Westphalia, 59423, DE |
| Mandatory US Agent | DREVE AMERICA CORP. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ESD |
| Regulation § (21 CFR) | 874.3300 |
| Proprietary names | Otopren; Tube end piece; Biopor AB; Fotoplast S hart; Biopor AB Xtrack; Thermosoft Lack; Fotoplast S IO lv; Biopor AB fluoreszent; BioTec; FotoTec Repair |
Source: openFDA. Public-domain (CC0).