Perfectio +

FDA UDI

Class II (US FDA UDI)

by Omm Imports Inc.

Identity

Trade Name: Perfectio + FDA UDI
Generic Name: Blue/red/infrared phototherapy lamp FDA UDI
Device Name: Over the counter red and infrared phototherapy device for the treatment of wrinkles. FDA UDI
Model / Reference: P900B FDA UDI
Description: Over the counter red and infrared phototherapy device for the treatment of wrinkles. FDA UDI

Identifiers

Primary DI / UDI-DI: 00850001456012 FDA UDI
FDA Product Code: OHS FDA UDI
GMDN Term: Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4810 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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Blue/red/infrared phototherapy lamp

Perfectio + by Omm Imports Inc. — 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: Omm Imports Inc.

Sources (1)

FDA UDI f4ab3320-fc31-4652-bc7d-1c3d1faf3e5f 34 fields · synced Jun 1, 2026