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Liceguard

FDA UDI

Class I (US FDA UDI)

by Liceguard, LLC

Identity

Trade Name
Liceguard FDA UDI
Generic Name
Lice removal/prevention kit FDA UDI
Model / Reference
Egg & Lice Combing Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00663580009209 FDA UDI
FDA Product Code
PUN FDA UDI
GMDN Term
Lice removal/prevention kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5960 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lice removal/prevention kit

Liceguard by Liceguard, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lice removal/prevention kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Liceguard, LLC

Sources (1)

  • FDA UDI c9457872-e32e-48b6-b2c3-b779d0a2d120 32 fields · synced May 30, 2026