Eclipse Pro 700-0390-00

GUDID 10841522129674

ECLIPSE PRO,DEFIB CABLE,PX,3 SNAP,LONG

SPACELABS HEALTHCARE (WASHINGTON), INC

Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable
Primary Device ID10841522129674
NIH Device Record Keyc7c03a17-b5b0-494b-a8a8-4fdd6547eea4
Commercial Distribution StatusIn Commercial Distribution
Brand NameEclipse Pro
Version Model NumberEclipse Pro
Catalog Number700-0390-00
Company DUNS145581588
Company NameSPACELABS HEALTHCARE (WASHINGTON), INC
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 Batchtrue
Serial Numberfalse
Manufacturing Datetrue
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
GS110841522129674 [Primary]

FDA Product Code

MWJElectrocardiograph, ambulatory (without analysis)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-07
Device Publish Date2024-02-28

On-Brand Devices [Eclipse Pro]

10841522128714ECLIPSE PRO,CABLE,PX,3 SNAP,SHORT
10841522127267ECLIPSE PRO,CABLE,PX,4 SNAP,MEDIUM
10841522129681ECLIPSE PRO,DEFIB CABLE,PX,3 SNAP,MEDIUM
10841522127281ECLIPSE PRO,CABLE,PX,10 SNAP,AHA
10841522129735ECLIPSE PRO,DEFIB CABLE,PX,10 SNAP,IEC
10841522128851ECLIPSE PRO RECORDER,MULTILINGUAL
10841522129711ECLIPSE PRO,DEFIB CABLE,PX,4 SNAP,MEDIUM
10841522129704ECLIPSE PRO,DEFIB CABLE,PX,4 SNAP,LONG
10841522129674ECLIPSE PRO,DEFIB CABLE,PX,3 SNAP,LONG
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.