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Kernel

FDA UDI

Class II (US FDA UDI)

by Xuzhou Kernel Medical Equipment Co., Ltd.

Identity

Trade Name
Kernel FDA UDI
Generic Name
Ultraviolet phototherapy unit, home-use FDA UDI
Model / Reference
KN-4006AL1D FDA UDI

Identifiers

Primary DI / UDI-DI
06928798600179 FDA UDI
510(k) Number
K181805 FDA UDI
FDA Product Code
FTC FDA UDI
GMDN Term
Ultraviolet phototherapy unit, home-use 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, home-use

Kernel by Xuzhou Kernel Medical Equipment Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultraviolet phototherapy unit, home-use.

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 fb202207-9be2-462e-9040-81fe3211801e 33 fields · synced May 30, 2026