Terumo Europe NV

Address:INTERLEUVENLAAN 40,LEUVEN Vlaams Brabant,BE

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

Needle, Hypodermic, Single Lumen (FMI) (10)

Premarket Exempt

Clear

K-Pack II - 05413206031771 Catalog Number : KN-2610RB

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 - 05413206031863 Catalog Number : KN-1838SBS

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 - 05413206032037 Catalog Number : KN-2232RB

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 - 05413206032648 Catalog Number : KN-2525RB04

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 - 05413206032655 Catalog Number : KN-2325RB04

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 - 05413206032662 Catalog Number : KN-2138RB04

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 - 05413206033201 Catalog Number : KN-2516RB05

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 - 05413206034321 Catalog Number : KN-2913RB

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 - 05413206034338 Catalog Number : KN-3013RB

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 - 05413206037087 Catalog Number : KN-2913RBS

Device Description : K-Pack II Needle

Device Class : 2

Duns Number: 370193559

Premarket Exempt : No

Product Code : FMI

Prescription Use : Yes

Device Count : 1

Previous 1 2 3 4 5 6 Next