Terumo Europe NV

Address:INTERLEUVENLAAN 40,LEUVEN Vlaams Brabant,BE

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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

Needle, Hypodermic, Single Lumen (FMI) (5) Set, Administration, Intravascular (FPA) (1)

Premarket Exempt

Clear

K-Pack II - 05413206223640 Catalog Number : KN-2713RKT50

Device Description : K-Pack II Needle

Device Class : 2

Duns Number: 370193559

Premarket Exempt : No

Product Code : FMI

Prescription Use : Yes

Device Count : 1

K-Pack II - 05413206223688 Catalog Number : KN-3013RKT50

Device Description : K-Pack II Needle

Device Class : 2

Duns Number: 370193559

Premarket Exempt : No

Product Code : FMI

Prescription Use : Yes

Device Count : 1

SURFLO® - 05413206246205 Catalog Number : SV-S25WL35C

Device Description : SURFLO® WINGED INFUSION SET WITH NEEDLE PROTECTION

Device Class :

Duns Number: 370193559

Premarket Exempt : No

Product Code : FPA

Prescription Use : Yes

Device Count : 1

K-Pack II - 05413206248216 Catalog Number : KN-2713RB500P

Device Description : K-Pack II Needle

Device Class :

Duns Number: 370193559

Premarket Exempt : No

Product Code : FMI

Prescription Use : Yes

Device Count : 1

K-Pack II Needle - 05413206250172 Catalog Number : KN-2719RBT500P

Device Description : K-Pack II Needle

Device Class :

Duns Number: 370193559

Premarket Exempt : No

Product Code : FMI

Prescription Use : Yes

Device Count : 1

K-Pack II - 05413206256532 Catalog Number : KN-2713RBK

Device Description : K-Pack II Needle

Device Class : 2

Duns Number: 370193559

Premarket Exempt : No

Product Code : FMI

Prescription Use : Yes

Device Count : 1

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