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National Biological Corporation

FDA UDI

Class II (US FDA UDI)

by National Biological Corp.

Identity

Trade Name
National Biological Corporation FDA UDI
Generic Name
Ultraviolet phototherapy unit, professional FDA UDI
Model / Reference
UVA-806 FDA UDI

Identifiers

Primary DI / UDI-DI
00816878020060 FDA UDI
510(k) Number
K827890 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

National Biological Corporation by National Biological Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K827890 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
National Biological Corp.

Sources (1)

  • FDA UDI 1e45e85d-ca21-42ab-bc36-d8b218cbdf3b 35 fields · synced May 30, 2026