17 results
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37ms
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Sources: EU EUDAMED, US FDA
CUREXO, INC.
Manufacturer
🇰🇷 South Korea·1 Basic UDI-DI·1 Device·BUREAU VERITAS ITALIA S.P.A.
CUREXO, Inc.
FDA registration
CUREXO, Inc.·2 products·🇰🇷 South Korea
Morning Walk
Device
EU MDD
·
Eu Md Class 2a
·CUREXO, INC.·On the market·1 country
CUVIS-spine Drape
FDA UDI
CUREXO, Inc.·08800043860768·
Morning Walk
FDA UDI
CUREXO, Inc.·08800043810121·
CUVIS-spine Drape
FDA UDI
CUREXO, Inc.·08800043860782·
CUVIS-spine
FDA UDI
CUREXO, Inc.·08800043830020·
N/A
FDA UDI
CUREXO, Inc.·08800043830006·
CUVIS-spine Drape
FDA UDI
CUREXO, Inc.·08800043860775·
Morning Walk
FDA UDI
CUREXO, Inc.·08800043810022·MW-S200
CUVIS-spine
FDA UDI
CUREXO, Inc.·08800043830013·
Morning Walk
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·CUREXO, INC.·1 device
IT288297
Certificate
MDD Annex II (excluding section 4)·CUREXO, INC.·BUREAU VERITAS ITALIA S.P.A.·1 Basic UDI-DI
Certification Experts
Authorized representative
🇳🇱 Netherlands·36 Manufacturers·3442 Devices
AR Experts B.V.
Authorized representative
🇳🇱 Netherlands·65 Manufacturers·3355 Devices
CMC Medical Devices & Drugs SL
Authorized representative
🇪🇸 Spain·698 Manufacturers·11260 Devices
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 23, 2024