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UltraPulse™ DUO

FDA UDI

Class II (US FDA UDI)

by Lumenis

Identity

Trade Name
UltraPulse™ DUO FDA UDI
Generic Name
General/multiple surgical solid-state/carbon dioxide laser system FDA UDI
Model / Reference
UltraPulse™ DUO FDA UDI

Identifiers

Catalog Number
GA-2000000D FDA UDI
Primary DI / UDI-DI
07290109147284 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical solid-state/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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General/multiple surgical solid-state/carbon dioxide laser system

UltraPulse™ DUO by Lumenis — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lumenis

Sources (1)

  • FDA UDI 5ccc9790-4bf3-4e3f-932a-c4b4c311c7de 33 fields · synced Jun 6, 2026