Posey Eye Protection

FDA UDI

Class I (US FDA UDI)

by Neolight Llc

Identity

Trade Name: Posey Eye Protection FDA UDI
Generic Name: Eye pad FDA UDI
Device Name: Eye protection for newborn phototherapy - sized for small/micro premie patients FDA UDI
Model / Reference: NL-EP-01S-MICRO FDA UDI
Description: Eye protection for newborn phototherapy - sized for small/micro premie patients FDA UDI

Identifiers

Primary DI / UDI-DI: 10852788008146 FDA UDI
FDA Product Code: FOK FDA UDI
GMDN Term: Eye pad FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5270 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Eye pad

Posey Eye Protection by Neolight Llc — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Neolight Llc

Sources (1)

FDA UDI 00cf415d-ddc0-4670-aebb-0b1e36c08792 33 fields · synced May 30, 2026