Delphi CF

GUDID 00815871022415

Avante

Fluoroscopy/angiography table top
Primary Device ID00815871022415
NIH Device Record Keydc24348d-9863-4352-915b-681a4af2a0bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameDelphi CF
Version Model Number70G6000
Company DUNS178440426
Company NameAvante
Device Count1
DM Exemptfalse
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

Customer Support Contacts

Phone502-244-4444
Emaildevicehelp@dremed.com
Phone502-244-4444
Emaildevicehelp@dremed.com
Phone502-244-4444
Emaildevicehelp@dremed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100815871022415 [Primary]

FDA Product Code

GDCTable, Operating-Room, Electrical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-06-19
Device Publish Date2018-04-17

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00815871020213 - Compact FM2020-03-02
00815871020220 - Compact FM2020-03-02
00815871020237 - Compact Plus2020-03-02
00815871020244 - Compact Plus2020-03-02
00815871020251 - Compact Plus2020-03-02

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