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Sony

FDA UDI

Class II (US FDA UDI)

by Sony Corporation

Identity

Trade Name
SONY FDA UDI
Generic Name
Operating room audiovisual data/device management system application software FDA UDI
Device Name
NUCLeUS OR Controller FDA UDI
Model / Reference
NU-MC30E FDA UDI
Description
NUCLeUS OR Controller FDA UDI

Identifiers

Primary DI / UDI-DI
04548736120679 FDA UDI
FDA Product Code
FTA FDA UDI
GMDN Term
Operating room audiovisual data/device management system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 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

Category: Operating room audiovisual data/device management system application software

Sony by Sony Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room audiovisual data/device management system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sony Corporation

Sources (1)

  • FDA UDI 7d4a4091-a189-45e0-acd2-a1f2d8a4c8ef 33 fields · synced May 30, 2026