NICO Myriad SPECTRA

FDA UDI

Class II (US FDA UDI)

by NICO Corporation

Identity

Trade Name: NICO Myriad SPECTRA FDA UDI
Generic Name: General-purpose light source FDA UDI
Device Name: NICO Myriad SPECTRA Light Source - US FDA UDI
Model / Reference: NN-7053 FDA UDI
Description: NICO Myriad SPECTRA Light Source - US FDA UDI

Identifiers

Catalog Number: NN-7053 FDA UDI
Primary DI / UDI-DI: 00816744027537 FDA UDI
FDA Product Code: QFX FDA UDI
GMDN Term: General-purpose light source FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4950 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: General-purpose light source

NICO Myriad SPECTRA by NICO Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: NICO Corporation

Sources (1)

FDA UDI d99ad001-5d12-4ddb-b0e6-e265e10bccea 35 fields · synced Jun 8, 2026