UDI device identifier

OPTIS™ Integrated System

UDI device identifier 00183739000937 · LIGHTLAB IMAGING, INC.

Key facts

Primary DI 00183739000937
Brand name OPTIS™
Version or model Integrated System
Catalog number C408652
Company LIGHTLAB IMAGING, INC.
DUNS number 018493531
Product code NQQ
GMDN term Coronary optical coherence tomography system
Device class Class II
Single use No
Packaged sterile No
Implantable No
Publish date Sep 28, 2015
Version date Feb 11, 2019
Description Imaging System

At a glance

  • 1–9 MAUDE reports citing this UDI
  • No Linked premarket submission
  • No EUDAMED counterpart found
  • 10–99 GUDID devices with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About UDI device identifiers (GUDID)

The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.

Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date:

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