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Quest Spectrum Platform

FDA UDI

Class II (US FDA UDI)

by Quest Projects B.V.

Identity

Trade Name
Quest Spectrum Platform FDA UDI
Generic Name
Surgical microscope fluorescent angiography system FDA UDI
Model / Reference
ART-SYS-0019 FDA UDI

Identifiers

Catalog Number
ART-SYS-0019 FDA UDI
Primary DI / UDI-DI
08719324487009 FDA UDI
FDA Product Code
GCJ FDA UDI
OWN FDA UDI
GMDN Term
Surgical microscope fluorescent angiography system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

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: Surgical microscope fluorescent angiography system

Quest Spectrum Platform by Quest Projects B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical microscope fluorescent angiography system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quest Projects B.V.

Sources (1)

  • FDA UDI cde476bc-d1f1-43ec-9534-5848849baf05 34 fields · synced Jun 8, 2026