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Planar LED mate

FDA UDI

Class II (US FDA UDI)

by Shenzhen Leaflife Technology Co., Ltd.

Identity

Trade Name
Planar LED mate FDA UDI
Generic Name
Intense pulsed light skin surface treatment system FDA UDI
Model / Reference
LH-LNIRS FDA UDI

Identifiers

Primary DI / UDI-DI
06974223650042 FDA UDI
FDA Product Code
OHT FDA UDI
GMDN Term
Intense pulsed light skin surface treatment system 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intense pulsed light skin surface treatment system

Planar LED mate by Shenzhen Leaflife Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intense pulsed light skin surface treatment system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shenzhen Leaflife Technology Co., Ltd.

Sources (1)

  • FDA UDI ff601233-4f60-4f2e-88ba-3882a13d34a0 32 fields · synced Jun 8, 2026