BIONIX DEVELOPMENT CORPORATION

Want to know more about this Organization? Request more information now!

Filters

Device Class

Class-1 (A medical device with low to moderate risk that requires general controls) Class-2 (A medical device with a moderate to high risk that requires special controls) Class-3 (A medical device with high risk that requires premarket approval) Class-U (Unclassified)

Product Code

blanket, neonatal phototherapy (PDH) (2) Gastrointestinal Tubes with Enteral Specific Connectors (PIF) (1) TUBES, GASTROINTESTINAL (AND ACCESSORIES) (KNT) (1)

Premarket Exempt

No Yes

Clear

BIONIX DEVELOPMENT CORPORATION - 10859911004273 Catalog Number : 1100

Device Description : Swaddler for PhotoTherapy, preemie

Device Class : 2

Duns Number: 602736795

Premarket Exempt : No

Product Code : PDH

Prescription Use : No

Device Count : 1

BIONIX DEVELOPMENT CORPORATION - 10859911004280 Catalog Number : 1105

Device Description : Swaddler for PhotoTherapy, normal

Device Class : 2

Duns Number: 602736795

Premarket Exempt : No

Product Code : PDH

Prescription Use : No

Device Count : 1

BIONIX DEVELOPMENT CORPORATION - 10859911004914 Catalog Number : 9510

Device Description : GASTROFLUSH 10CT.

Device Class : 2

Duns Number: 602736795

Premarket Exempt : No

Product Code : KNT, PIF

Prescription Use : Yes

Device Count : 1

Previous 1 2 3 4 Next