FDA Device Entity Profile: RUDOLF RIESTER GMBH & CO. KG

Known Identifiers & Locations

FEI Numbers 1000292048

Owner Operator Numbers 8010492

Locations Covered JUNGINGEN Baden-Wurttemberg, DE

Registered Establishments (1)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
8010482	RUDOLF RIESTER GMBH	JUNGINGEN Baden-Wurttemberg, DE	Manufacture Medical Device	View Details

510(k) Premarket Notifications (2)

Submission #	Device Name	Decision Date	Decision Description	Action
K932506	RI-SCOPE (S)	1993-10-08	Substantially Equivalent	View Details
K972301	BIG BEN SQUARE, BIG BEN ROUND	1997-09-17	Substantially Equivalent	View Details

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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