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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
3 SERIES PC 311-24 FDA UDI
Model / Reference
3 SERIES PC FDA UDI
Description
3 SERIES PC 311-24 FDA UDI

Identifiers

Catalog Number
861PH0024PC6 FDA UDI
Primary DI / UDI-DI
B280861PH0024PC60 FDA UDI
510(k) Number
K063621 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

K063621 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 9027f774-a69b-4c70-b297-a00238cc04b6 37 fields · synced May 31, 2026