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Domino

FDA UDIEUDAMED

Class II (US FDA UDI)

by Quanta System Spa

Identity

Trade Name
Domino FDA UDI
Generic Name
Dermatological frequency-doubled solid-state laser system FDA UDI
Model / Reference
PAMS00033 FDA UDI

Identifiers

Primary DI / UDI-DI
08033945934088 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Dermatological frequency-doubled solid-state 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dermatological frequency-doubled solid-state laser system

Domino by Quanta System Spa — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological frequency-doubled solid-state laser system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quanta System Spa

Sources (2)

  • FDA UDI 8fc2ac02-a725-4f42-8525-3c95fcc861ae 32 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026