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Symphony Oct System

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 1020-35-114Model SYMPHONY OCT System - Screws

by Medos International SARL

Identity

Trade Name
SYMPHONY OCT SYSTEM EUDAMED
SYMPHONY FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Screws for Cervical Fixation System EUDAMED
SYMPHONY OCT SYSTEM POLYAXIAL SCREW Diameter 4.0 Rod, 3.5X14mm FDA UDI
Model / Reference
SYMPHONY OCT System - Screws EUDAMED
1020-35-114 EUDAMEDFDA UDI
Description
SYMPHONY OCT SYSTEM POLYAXIAL SCREW Diameter 4.0 Rod, 3.5X14mm FDA UDI

Identifiers

Catalog Number
102035114 FDA UDI
Primary DI / UDI-DI
10705034508696 EUDAMEDFDA UDI
Basic UDI-DI
0705034a0023663 EUDAMED
510(k) Number
K181949 FDA UDI
K190895 FDA UDI
FDA Product Code
KWP FDA UDI
NKG FDA UDI
EMDN Code
P09070301 CERVICAL FIXATION SYSTEMS EUDAMED
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
888.3075 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Cervical spine immobilization system, single-use

Symphony Oct 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 3f4aa458-0a70-4bbc-bf81-c72b03a818f1 61 fields · synced Jul 23, 2026
  • FDA UDI 5940cba7-0100-4693-b780-a2613c70d83b 36 fields · synced May 30, 2026