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Bvlaser

FDA UDI

Class II (US FDA UDI)

by Nanjing Bestview Laser S&T Co., Ltd.

Identity

Trade Name
BVLASER FDA UDI
Generic Name
General/multiple surgical carbon dioxide laser system FDA UDI
Device Name
The CO2 Laser Machine is used for body soft tissue vaporization and coagulation in dermatology and plastic surgery, general surgery, gynecology. FDA UDI
Model / Reference
Lume FDA UDI
Description
The CO2 Laser Machine is used for body soft tissue vaporization and coagulation in dermatology and plastic surgery, general surgery, gynecology. FDA UDI

Identifiers

Primary DI / UDI-DI
06974851082062 FDA UDI
510(k) Number
K250465 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical carbon dioxide 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General/multiple surgical carbon dioxide laser system

Bvlaser by Nanjing Bestview Laser S&T Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General/multiple surgical carbon dioxide laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6c4db28f-48f5-4946-88db-1d8a6d66b864 34 fields · synced Jun 9, 2026