Myriad-LX

FDA UDI

Class II (US FDA UDI)

by NICO Corporation

Identity

Trade Name: Myriad-LX FDA UDI
Generic Name: Electrical mains power cable FDA UDI
Model / Reference: NN-7023 FDA UDI

Identifiers

Primary DI / UDI-DI: 00816744027230 FDA UDI
510(k) Number: K191599 FDA UDI
FDA Product Code: FTD FDA UDI
GMDN Term: Electrical mains power cable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrical mains power cable

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

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Sklar® — Sklar Corporation · Class II

Cleared under the same submission

K191599 also covers:

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 60919366-914d-4ac9-a314-bedd229cb724 33 fields · synced Jun 1, 2026