Replacement Kit for CHARGE-PAK battery charger 11403-000002

GUDID 00721902514128

SHIPPING ASSY-C-P, Q-P,REPL KIT, 1 ELECTRODE

PHYSIO-CONTROL, INC.

Rechargeable public semi-automated external defibrillator Rechargeable public semi-automated external defibrillator
Primary Device ID00721902514128
NIH Device Record Key6ba3fe61-e033-4f4f-876b-2e2293e6ece6
Commercial Distribution StatusIn Commercial Distribution
Brand NameReplacement Kit for CHARGE-PAK battery charger
Version Model Number11403
Catalog Number11403-000002
Company DUNS009251992
Company NamePHYSIO-CONTROL, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)442-1142
Emailrs.seacustomersupport@physio-control.com
Phone+1(800)442-1142
Emailrs.seacustomersupport@physio-control.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100721902514128 [Primary]

FDA Product Code

MKJAutomated external defibrillators (non-wearable)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2014-11-10

On-Brand Devices [Replacement Kit for CHARGE-PAK battery charger]

00721902514128SHIPPING ASSY-C-P, Q-P,REPL KIT, 1 ELECTRODE
00883873824597SHIPPING ASSY-C-P, Q-P,REPL KIT, 1 ELECTRODE

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