FDA.reportPublic FDA data

DIVA LABORATORIES, LTD.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30078170023007817002DIVA LABORATORIES, LTD.1N2020-04-259F. NO.351, SEC.2 ZHONGSHAN ROAD ZHONGHE DIST. NEW TAIPEI CITY, TAIPEI-DISTRICT, 235 Ta TW 235

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
04719875210211DIVA - GUP2103CMI973-983-8809kevin_chen@diva.com.tw
04719875210525DIVA - ZSP2105CMI973-983-8809kevin_chen@diva.com.tw

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1068392066791660K191705OptikView GUP2103CMIPGY2020-03-16
1068391770900112K160328DIVA ZSP2105CMI with QUBYX PerfectLum bundlePGY2016-02-25
1068391680967505K152847DIVA ZSP5812CMI with QUBYX PerfectLum bundlePGY2015-11-17
1068391052206158
1068391406319717
1068391540040386

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PGY32020-03-16

GUDID#