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Led Light Phototherapy Bed

FDA UDI

Class II (US FDA UDI)

by Shenzhen Suyzeko Limited.

Identity

Trade Name
Led Light Phototherapy Bed FDA UDI
Generic Name
Red/infrared light phototherapy unit FDA UDI
Model / Reference
Pro450 FDA UDI

Identifiers

Primary DI / UDI-DI
06973337184504 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Red/infrared light phototherapy unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Red/infrared light phototherapy unit

Led Light Phototherapy Bed by Shenzhen Suyzeko Limited. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Red/infrared light phototherapy unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 68326d46-87f8-4206-b430-3a5a293cd220 32 fields · synced May 30, 2026