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Advanced Led Phototherapy Lamp

FDA UDI

Class II (US FDA UDI)

by Advanced Instrumentations, Inc.

Identity

Trade Name
ADVANCED LED PHOTOTHERAPY LAMP FDA UDI
Generic Name
Overhead infant phototherapy unit FDA UDI
Model / Reference
PT-5000 FDA UDI

Identifiers

Primary DI / UDI-DI
B510PT5000 FDA UDI
FDA Product Code
LBI FDA UDI
GMDN Term
Overhead infant phototherapy unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5700 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

No

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

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: Overhead infant phototherapy unit

Advanced Led Phototherapy Lamp by Advanced Instrumentations, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Overhead infant phototherapy unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 441ca447-6c21-4d75-9e23-4f165bdf1673 32 fields · synced May 30, 2026