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Beurer

FDA UDI

Class I (US FDA UDI)

by Beurer North America, L.p.

Identity

Trade Name
Beurer FDA UDI
Generic Name
Lice comb, powered FDA UDI
Device Name
Lice Comb (Powered) FDA UDI
Model / Reference
HT15 FDA UDI
Description
Lice Comb (Powered) FDA UDI

Identifiers

Catalog Number
Art.- No. 591.71 FDA UDI
Primary DI / UDI-DI
00853879007935 FDA UDI
FDA Product Code
LJL FDA UDI
GMDN Term
Lice comb, powered 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lice comb, powered

Beurer by Beurer North America, L.p. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lice comb, powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b9b24f14-d1bd-4a42-87be-2dcd427a8a25 35 fields · synced Jun 8, 2026