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Sunoptic Surgical, CUDA, Sunoptic Technologies, OEM Customer

FDA UDI

Class II (US FDA UDI)

by Sunoptic Technologies

Identity

Trade Name
Sunoptic Surgical, CUDA, Sunoptic Technologies, OEM Customer FDA UDI
Generic Name
General-purpose light source FDA UDI
Device Name
Xenon Lightsource, 300 Watt, Digital FDA UDI
Model / Reference
DPLS-01, DPLS-03 FDA UDI
Description
Xenon Lightsource, 300 Watt, Digital FDA UDI

Identifiers

Primary DI / UDI-DI
M678DPLS300W0 FDA UDI
FDA Product Code
FSS FDA UDI
GMDN Term
General-purpose light source FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 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

Yes

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-purpose light source

Sunoptic Surgical, CUDA, Sunoptic Technologies, OEM Customer by Sunoptic Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose light source.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 27046477-90ca-43d1-ae79-fc016eccde65 33 fields · synced Jun 8, 2026