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Skyline Anterior Cervical Plate System

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 186801024SModel SKYLINE Anterior Cervical Plate System Plates

by Medos International SARL

Identity

Trade Name
SKYLINE ANTERIOR CERVICAL PLATE SYSTEM EUDAMED
SKYLINE FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
Plates EUDAMED
SKYLINE ANTERIOR CERVICAL PLATE SYSTEM ONE LEVEL PLATE 24mm FDA UDI
Model / Reference
SKYLINE Anterior Cervical Plate System Plates EUDAMED
186801024S EUDAMEDFDA UDI
Description
SKYLINE ANTERIOR CERVICAL PLATE SYSTEM ONE LEVEL PLATE 24mm FDA UDI

Identifiers

Catalog Number
186801024S FDA UDI
Primary DI / UDI-DI
10705034411897 EUDAMEDFDA UDI
Basic UDI-DI
0705034a002215N EUDAMED
510(k) Number
K132324 FDA UDI
K171439 FDA UDI
FDA Product Code
KWQ FDA UDI
EMDN Code
P09070301 CERVICAL FIXATION SYSTEMS EUDAMED
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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
MRI Safety
MR Conditional FDA UDI

Category: Cervical spine immobilization system, single-use

Skyline Anterior Cervical Plate System by Medos International Sarl — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cervical spine immobilization system, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CH-MF-000014268
Authorised Representative
DePuy Ireland UC IE-AR-000009328

Sources (2)

  • EUDAMED 89a4e26a-b058-433f-9d4a-9aaeed1a4d21 61 fields · synced Jul 11, 2026
  • FDA UDI 771fd2f0-2990-45c6-85c6-58543400fb80 36 fields · synced May 30, 2026