Lifeline View

GUDID 00815098020232

DEFIBTECH, L.L.C.

Non-rechargeable public semi-automated external defibrillator
Primary Device ID00815098020232
NIH Device Record Keyab4b0250-776a-4dce-80bc-24102c74b99a
Commercial Distribution StatusIn Commercial Distribution
Brand NameLifeline View
Version Model NumberDDU-E2300
Company DUNS128340200
Company NameDEFIBTECH, L.L.C.
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 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
GS100815098020232 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

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 Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

On-Brand Devices [Lifeline View]

00815098020232DDU-E2300
00815098020201DDU-A2300

Trademark Results [Lifeline View]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LIFELINE VIEW
LIFELINE VIEW
85157952 4069607 Live/Registered
Defibtech, LLC
2010-10-21

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