Diagnostica Stago - Taverny
Taverny Val-d'Oise, FR
Diagnostica Stago - Taverny appears in FDA device records in Taverny Val-d'Oise, FR. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 1
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 9710666 | 3003565434 | Diagnostica Stago - Taverny | 23/29 rue Constantin Pecqueur, Taverny Val-d'Oise 95150 FR | 2026 | and 14 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- GFOActivated Partial Thromboplastin
- JBXAggregrometer, Platelet
- JBQAntithrombin Iii Quantitation
- KFFAssay, Heparin
- JCOBothrops Atrox Reagent
- JISCalibrator, Primary
- GGCControl, Plasma, Abnormal
- JLAConversion To Creatinine, Creatine
- JBNFibrin Monomer Paracoagulation
- GHHFibrin Split Products
- DAPFibrinogen And Fibrin Split Products, Antigen, Antiserum, Control
- PPMGeneral Purpose Reagent
- GGNPlasma, Coagulation Control
- GJTPlasma, Coagulation Factor Deficient
- GIZPlasma, Control, Normal
- DDXPlasminogen, Antigen, Antiserum, Control
- LCOPlatelet Factor 4 Radioimmunoassay
- GIRReagent, Russel Viper Venom
- KQJSystem, Fibrinogen Determination
- GGPTest, Qualitative And Quantitative Factor Deficiency
- GJATest, Thrombin Time
- GGWTest, Time, Partial Thromboplastin
- GJSTest, Time, Prothrombin
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
