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Full Body Unit, 44 UVA Lamp Unit

FDA UDI

Class II (US FDA UDI)

by Ultralite Enterprises Inc

Identity

Trade Name
Full Body Unit, 44 UVA Lamp Unit FDA UDI
Generic Name
Ultraviolet phototherapy unit, professional FDA UDI
Model / Reference
V4400 FDA UDI

Identifiers

Primary DI / UDI-DI
B276V44000 FDA UDI
FDA Product Code
FTC FDA UDI
GMDN Term
Ultraviolet phototherapy unit, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4630 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

Yes

FDA UDI

Category: Ultraviolet phototherapy unit, professional

Full Body Unit, 44 UVA Lamp Unit by Ultralite Enterprises Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultraviolet phototherapy unit, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ultralite Enterprises Inc

Sources (1)

  • FDA UDI ec6d8e61-f8aa-4965-bc01-8cc3cf0df7bf 33 fields · synced May 31, 2026