Hoogland Spine Products GmbH

Address:Feringastr. 4,Unterfoehring Munich Bavaria,DE

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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

Bit, Drill (HTW) (6) Guide, Needle, Surgical (GDF) (2) Forceps (HTD) (1) Wrench (HXC) (1)

Premarket Exempt

No Yes

Clear

MaxMoreSpine - 04260200310125 Catalog Number :

Device Description : Manual Bone Drill 7 mm

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : HTW

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310149 Catalog Number :

Device Description : Manual Bone Drill 8 mm

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : HTW

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310163 Catalog Number :

Device Description : Manual Bone Drill 9 mm

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : HTW

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310187 Catalog Number :

Device Description : Manual Bone Mill

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : HTW

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310194 Catalog Number :

Device Description : Tappet

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : HTW

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310217 Catalog Number :

Device Description : Manual Bone Drill 5 mm, steril

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : HTW

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310224 Catalog Number :

Device Description : Ball Handle

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : HXC

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310231 Catalog Number :

Device Description : Cervical Dilator 4,0 mm

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : GDF

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310248 Catalog Number :

Device Description : Cervical Dilator Head

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : GDF

Prescription Use : No

Device Count : 1

MaxMoreSpine - 04260200310255 Catalog Number :

Device Description : Cervical Forceps Ø 1,7 mm, 270 mm

Device Class : 1

Duns Number: 507292204

Premarket Exempt : Yes

Product Code : HTD

Prescription Use : No

Device Count : 1

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