Terumo Europe NV

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) (10)

Premarket Exempt

No

Clear

K-Pack II - 05413206003785 Catalog Number : KN-1838SB

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 - 05413206003792 Catalog Number : KN-2325RB

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 - 05413206003808 Catalog Number : KN-2516RB04

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 - 05413206003815 Catalog Number : KN-2525RB

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 - 05413206018147 Catalog Number : KN-2138RB

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 - 05413206020546 Catalog Number : KN-2713RB

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 - 05413206025053 Catalog Number : KN-2332RB

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 - 05413206031160 Catalog Number : KN-2713RBR

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 - 05413206031313 Catalog Number : KN-2238RB

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 - 05413206031740 Catalog Number : KN-1938RB

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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