Data / Medical devices / Respiratory Syncytial Virus - Elisa
Respiratory Syncytial Virus - Elisa (MCE): 4 FDA-registered makers in 2 countries
4 establishments in 2 countries are registered with the FDA to make Respiratory Syncytial Virus - Elisa (product code MCE, Class 1, 21 CFR 866.3480). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on September 8, 2006, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MCE
- Device class
- 1
- Regulation
- 866.3480
- Medical specialty
- Microbiology
Makers by country
| Country | Makers |
|---|---|
| Germany | 3 |
| China | 1 |
Makers of Respiratory Syncytial Virus - Elisa
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| DRG Instruments GMBH | MARBURG Hesse, Germany | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Euroimmun Medizinische Labordiagnostika AG | Luebeck Schleswig-Holstein, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| EUROIMMUN Medizinische Labordiagnostika AG | Dassow Mecklenburg-Western Pomerania, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yiwu Daqida Plastic Products Co., Ltd. | Yiwu Zhejiang, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated September 8, 2006. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.