DA200P40+LMB 9890-000-87251

GUDID 00884838102613

diagnostic x-ray tube housing assembly

Philips Medical Systems DMC GmbH

X-ray tube housing assembly, diagnostic
Primary Device ID00884838102613
NIH Device Record Keyeb647b20-e905-45dc-b3dd-6378626297ad
Commercial Distribution StatusIn Commercial Distribution
Brand NameDA200P40+LMB
Version Model Number9890-000-87251
Catalog Number9890-000-87251
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
GS100884838102613 [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 Date2020-12-04
Device Publish Date2020-11-26

Devices Manufactured by Philips Medical Systems DMC GmbH

00884838125322 - Grid Landscape for SkyPlate E 2025-06-27
00884838125339 - Grid Landscape for SkyPlate large 2025-06-27
00884838125346 - Grid Portrait for SkyPlate E 2025-06-27
00884838125353 - Grid Portrait for SkyPlate large2025-06-27
00884838125360 - Grid Portrait for SkyPlate small 2025-06-27
00884838125384 - Grid Portrait Fiber PaxScan4336W2025-06-27
00884838125391 - Grid Landscape Fiber PaxScan4336W2025-06-27
00884838125421 - X-Ray Grid 40/12/1402025-06-27

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.