FDA.reportPublic FDA data

JOLIFE AB

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30054457173005445717JOLIFE AB1N2026-01-01IDEON SCIENCE PARK SCHEELEVAGEN 17 LUND Skane SE 22370

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00883873826300LUCAS CHEST COMPRESSION SYSTEM - USED LUCAS 3, 3.1, IN SHIPPING BOX, EN+1(800)442-1142rs.seacustomersupport@physio-control.com
00883873826584LUCAS CHEST COMPRESSION SYSTEM - USED LUCAS 3, 3.0, IN SHIPPING BOX, EN+1(800)442-1142rs.seacustomersupport@physio-control.com
00883873834282LUCAS CPR Chest Compression System - LUCAS 3, 3.1, IN SHIPPING BOX, JA+1(800)442-1142rs.seacustomersupport@stryker.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2140331693779687K173553LUCAS 3 Chest Compression SystemDRM2018-02-08
2140331041100631K161768LUCAS 3 Chest Compression SystemDRM2016-11-09
2140331823593467K090422LUCAS 2DRM2009-06-17
2140331319339521K062401MODIFICATION TO LUCASDRM2006-09-28
2140331153879390K053403LUCASDRM2006-02-01

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DRM52018-02-08

PMN#

GUDID#