vMRC Performance 9890-000-87381

GUDID 00884838107168

diagnostic x-ray tube housing assembly

Philips Medical Systems DMC GmbH

X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic X-ray tube housing assembly, diagnostic
Primary Device ID00884838107168
NIH Device Record Keya2f807ea-ddd4-4f0f-ace2-9bb2f38bfb0a
Commercial Distribution StatusIn Commercial Distribution
Brand NamevMRC Performance
Version Model Number9890-000-87381
Catalog Number9890-000-87381
Company DUNS314101218
Company NamePhilips Medical Systems DMC GmbH
Device Count1
DM Exempttrue
Pre-market Exempttrue
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100884838107168 [Primary]

FDA Product Code

ITYAssembly, tube housing, x-ray, diagnostic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-08
Device Publish Date2021-06-30

On-Brand Devices [vMRC Performance]

00884838085589diagnostic x-ray tube housing assembly
00884838107168diagnostic x-ray tube housing assembly
00884838120501diagnostic x-ray tube housing assembly

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.