BAUI BIOTECH CO. LTD.

Address:6F., No.8, Sec.1, Zhongxing Rd.,New Taipei City,TW

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

Intervertebral Fusion Device With Bone Graft, Lumbar (MAX) (7) Thoracolumbosacral Pedicle Screw System (NKB) (3)

Premarket Exempt

Clear

COMET Lumbar Interbody Fusion Cage - 04710577041493 Catalog Number :

Device Description : PEEK Interbody Fusion Cage

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : MAX

Prescription Use : No

Device Count : 1

COMET Lumbar Interbody Fusion Cage - 04710577041509 Catalog Number :

Device Description : PEEK Interbody Fusion Cage

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : MAX

Prescription Use : No

Device Count : 1

COMET Lumbar Interbody Fusion Cage - 04710577041516 Catalog Number :

Device Description : PEEK Interbody Fusion Cage

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : MAX

Prescription Use : No

Device Count : 1

COMET Lumbar Interbody Fusion Cage - 04710577041523 Catalog Number :

Device Description : PEEK Interbody Fusion Cage

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : MAX

Prescription Use : No

Device Count : 1

COMET Lumbar Interbody Fusion Cage - 04710577041530 Catalog Number :

Device Description : PEEK Interbody Fusion Cage

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : MAX

Prescription Use : No

Device Count : 1

COMET Lumbar Interbody Fusion Cage - 04710577041547 Catalog Number :

Device Description : PEEK Interbody Fusion Cage

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : MAX

Prescription Use : No

Device Count : 1

COMET Lumbar Interbody Fusion Cage - 04710577041554 Catalog Number :

Device Description : PEEK Interbody Fusion Cage

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : MAX

Prescription Use : No

Device Count : 1

NOVA Minimally Invasive System - 04712899252717 Catalog Number :

Device Description : Pre-Bent Rod

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : NKB

Prescription Use : No

Device Count : 1

NOVA Minimally Invasive System - 04712899252724 Catalog Number :

Device Description : Pre-Bent Rod

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : NKB

Prescription Use : No

Device Count : 1

NOVA Minimally Invasive System - 04712899252731 Catalog Number :

Device Description : Pre-Bent Rod

Device Class : 2

Duns Number: 656775504

Premarket Exempt : No

Product Code : NKB

Prescription Use : No

Device Count : 1

Previous 1 2 3 4 5 … 42 Next