30 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113486·MINIATURE BLADE #65 (BX/5)
Night Guard
FDA 510(k)
FDA Unclassified
·Unknown
nSpire Health
FDA UDI
NSPIRE HEALTH, INC.·10852417003696·KoKo Standard White Filter Kit with Nose Clip a...
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668113394·MICS TRAP KNIFE 1.8/2.2 (BX/5)
Blade Scalpel
FDA UDI
KATENA PRODUCTS, INC.·00841668113479·MINIATURE BLADE #64 (BX/5)
SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876
FDA 510(k)
FDA Class 2
·Anesthesiology
MODIFICATION TO NASAL-AIRE
FDA 510(k)
FDA Class 2
·Anesthesiology
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC·Product code GJS·September 21, 2012
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·January 10, 2024
BIPAP A30
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 31, 2022
BIPAP ST
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP ST
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP AVAPS
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP ST
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 3, 2022
BIPAP A30
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP AVAPS
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP ST
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022
BIPAP A30
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 30, 2022
BIPAP AVAPS
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 16, 2022
BIPAP AVAPS
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 20, 2022