GUDID 00195278569745

BB X-RAY OVERHEAD TUBE SUSPENSION

Hangwei GE Medical Systems Co., Ltd.

Stationary basic diagnostic x-ray system, digital
Primary Device ID00195278569745
NIH Device Record Key3fae79f8-9837-4544-b645-a221da0f27a5
Commercial Distribution StatusIn Commercial Distribution
Version Model Number5135678-10
Company DUNS654659689
Company NameHangwei GE Medical Systems Co., Ltd.
Device Count1
DM Exempttrue
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 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
GS100195278569745 [Primary]

FDA Product Code

IYBTube mount, 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 Date2022-07-29
Device Publish Date2022-07-21

Devices Manufactured by Hangwei GE Medical Systems Co., Ltd.

00195278913807 - Definium2024-11-07 Definium Pace Select ET System UDI
00195278832252 - NA2024-07-09 Galaxy 2.0 Wall Stand(Insert Left)
00195278798107 - Revolution2024-03-07 Revolution Ascend Sliding designated medical device
00195278788665 - Revolution Apex2024-01-03 Revolution Apex Select with Plus Edition - Designated System Medical Device
00195278526892 - Definium2023-09-26 Definium Pace Select system designated medical device
00195278713759 - NA2023-09-26 Galaxy 2.0 Wall Stand
00195278713766 - NA2023-09-26 Value Fixed Table
00195278686718 - Revolution2023-06-30 Revolution Maxima CT designated medical device

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