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Verticale

FDA UDI

Class II (US FDA UDI)

by Silony Medical GmbH

Identity

Trade Name
VERTICALE FDA UDI
Generic Name
Bone-screw internal spinal fixation system, sterile FDA UDI
Device Name
VERTICALE Iliac Screw 9.2x50 mm, can+fen FDA UDI
Model / Reference
S-VIS-9250-KF1 FDA UDI
Description
VERTICALE Iliac Screw 9.2x50 mm, can+fen FDA UDI

Identifiers

Primary DI / UDI-DI
04054896047485 FDA UDI
FDA Product Code
NKB FDA UDI
KWP FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 9.2 Millimeter FDA UDI
Length — 50 Millimeter FDA UDI

Category: Bone-screw internal spinal fixation system, sterile

Verticale by Silony Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Silony Medical GmbH

Sources (1)

  • FDA UDI 17727ffe-7433-48a0-8439-40f2d1f01dcb 34 fields · synced May 30, 2026