N33 CCD System N331N0CL1

GUDID 08056600520594

NICAL SPA

Fluoroscopic x-ray system video image recording unit
Primary Device ID08056600520594
NIH Device Record Key6e8dca7d-5745-4722-ae6f-31eec14b37b4
Commercial Distribution StatusIn Commercial Distribution
Brand NameN33 CCD System
Version Model NumberN33
Catalog NumberN331N0CL1
Company DUNS435743877
Company NameNICAL SPA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108056600520594 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JAASystem, X-Ray, Fluoroscopic, Image-Intensified

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-19
Device Publish Date2023-10-11

On-Brand Devices [N33 CCD System]

08056600521324N33
08056600520884N33
08056600520877N33
08056600520860N33
08056600520853N33
08056600520846N33
08056600520839N33
08056600520822N33
08056600520815N33
08056600520808N33
08056600520792N33
08056600520785N33
08056600520778N33
08056600520761N33
08056600520754N33
08056600520747N33
08056600520730N33
08056600520723N33
08056600520716N33
08056600520709N33
08056600520693N33
08056600520686N33
08056600520679N33
08056600520662N33
08056600520655N33
08056600520648N33
08056600520631N33
08056600520624N33
08056600520617N33
08056600520600N33
08056600520594N33
08056600520587N33
08056600520570N33
08056600520563N33
08056600520556N33
08056600520549N33

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