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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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96 records meeting your search criteria returned- Product Code: HAB Product Problem: Device Inoperable Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
ZIMMER SURGICAL SA MODULAR ELECTRIC/BATTERY DOUBLE TRIGGER 06/05/2018
ZIMMER SURGICAL SA MODULAR ELECTRIC/BATTERY DOUBLE TRIGGER 06/05/2018
SMITH & NEPHEW, INC. MOTOR DRIVE UNIT, HAND CNTRL, PWRMX EL 05/22/2018
SMITH & NEPHEW, INC. RFB, MDU, HAND CNTRL, PWRMX EL 05/15/2018
SMITH & NEPHEW, INC. SVC REPL MDU HAND CNTRL PWRMX 05/15/2018
SMITH & NEPHEW, INC. MOTOR DRIVE UNIT, HAND CNTRL, PWRMX EL 05/10/2018
SMITH & NEPHEW, INC. MOTOR DRIVE UNIT, HAND CNTRL, PWRMX EL 04/29/2018
SMITH & NEPHEW, INC. MOTOR DRIVE UNIT, HAND CNTRL, PWRMX EL 04/27/2018
SMITH & NEPHEW, INC. SVC REPL MDU HAND CNTRL PWRMX 04/16/2018
ZIMMER SURGICAL SA MODULAR ELECTRIC/BATTERY DOUBLE TRIGGER 03/28/2018
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