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Symphony

FDA UDI

Class I (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
SYMPHONY FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
SYMPHONY OCT SYSTEM POLYAXIAL SCREW DRIVER SHAFT X20, CANNULATED, SHORT FDA UDI
Model / Reference
2020-00-355 FDA UDI
Description
SYMPHONY OCT SYSTEM POLYAXIAL SCREW DRIVER SHAFT X20, CANNULATED, SHORT FDA UDI

Identifiers

Catalog Number
202000355 FDA UDI
Primary DI / UDI-DI
10705034530819 FDA UDI
FDA Product Code
HXX FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

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

Category: Surgical screwdriver, reusable

Symphony by Medos International Sàrl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 51c7c742-1d3b-4e05-becb-4a89d57ca39a 35 fields · synced Jun 1, 2026