Diode Laser Hair Removal machine

FDA UDI

Class II (US FDA UDI)

by Beijing Nubway S&T Co., Ltd.

Identity

Trade Name: Diode Laser Hair Removal machine FDA UDI
Generic Name: Dermatological diode laser system FDA UDI
Model / Reference: QDTM-01 FDA UDI

Identifiers

Primary DI / UDI-DI: 06971679500013 FDA UDI
510(k) Number: K192735 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dermatological diode laser system

Diode Laser Hair Removal machine by Beijing Nubway S&T Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Beijing Nubway S&T Co., Ltd.

Sources (1)

FDA UDI 362d4c36-193c-4471-944c-1804f4f0a62a 33 fields · synced Jun 9, 2026