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Handisol

FDA UDI

Class II (US FDA UDI)

by Daavlin Distributing Co., The

Identity

Trade Name
Handisol FDA UDI
Generic Name
Ultraviolet phototherapy unit, professional FDA UDI
Device Name
UVB-150-2 FDA UDI
Model / Reference
Handisol FDA UDI
Description
UVB-150-2 FDA UDI

Identifiers

Primary DI / UDI-DI
00850054882066 FDA UDI
510(k) Number
K233811 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

No

FDA UDI

Category: Ultraviolet phototherapy unit, professional

Handisol by Daavlin Distributing Co., The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultraviolet phototherapy unit, professional.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 257c2e7a-d2ae-4ab1-950e-64213cf1d8c2 35 fields · synced May 30, 2026