ProxiDiagnost N90

GUDID 00884838103221

Philips Medical Systems DMC GmbH

Stationary general-purpose fluoroscopic x-ray system, digital
Primary Device ID00884838103221
NIH Device Record Key84a016c4-49c8-4a37-8ae5-0a6a042de282
Commercial Distribution StatusIn Commercial Distribution
Brand NameProxiDiagnost N90
Version Model Number706110
Company DUNS314101218
Company NamePhilips Medical Systems DMC GmbH
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 Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100884838103221 [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 Date2022-01-25
Device Publish Date2022-01-17

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