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Bestview

FDA UDI

Class II (US FDA UDI)

by Zhengzhou Bestview ST Co., Ltd.

Identity

Trade Name
Bestview FDA UDI
Generic Name
Dermatological diode laser system FDA UDI
Device Name
The Diode Laser Machine (Model: BM-100) is intended for hair removal, permanent hair reduction on all skin types (Fitzpatrick skin type I-VI), including tanned skin. FDA UDI
Model / Reference
BM-100 FDA UDI
Description
The Diode Laser Machine (Model: BM-100) is intended for hair removal, permanent hair reduction on all skin types (Fitzpatrick skin type I-VI), including tanned skin. FDA UDI

Identifiers

Primary DI / UDI-DI
06974892091016 FDA UDI
510(k) Number
K211335 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Dermatological diode laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dermatological diode laser system

Bestview by Zhengzhou Bestview ST Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological diode laser system.

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 e9cd6fc4-35ba-4836-9e1b-6bc788f60042 34 fields · synced May 30, 2026