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Daavlin

FDA UDI

Class II (US FDA UDI)

by Daavlin Distributing Co., The

Identity

Trade Name
DAAVLIN FDA UDI
Generic Name
Ultraviolet phototherapy unit, professional FDA UDI
Device Name
DIGITAL DERMAPAL UVA 120V 60HZ FDA UDI
Model / Reference
DIGITAL DERMAPAL FDA UDI
Description
DIGITAL DERMAPAL UVA 120V 60HZ FDA UDI

Identifiers

Catalog Number
935DPADT60 FDA UDI
Primary DI / UDI-DI
B280935DPADT600 FDA UDI
510(k) Number
K073587 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
Not 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

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

Cleared under the same submission

K073587 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Daavlin Distributing Co., The

Sources (1)

  • FDA UDI 0648e833-2f03-4498-8e83-e037d99f1a1d 37 fields · synced Jun 8, 2026