iLifeplus

GUDID B459SY18220

PURE LIFE SOLUTIONS INC.

Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin Infrared patient thermometer, skin
Primary Device IDB459SY18220
NIH Device Record Key7c8e47a4-d98e-4ae9-9ef7-d1ee1ffc0d97
Commercial Distribution StatusIn Commercial Distribution
Brand NameiLifeplus
Version Model NumberJPD-FR200
Company DUNS080406332
Company NamePURE LIFE SOLUTIONS 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 Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com
Phone619-324-9680
Emailpurelifesolution@gmail.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB459SY18220 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FLLThermometer, Electronic, Clinical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-06-03
Device Publish Date2019-05-24

On-Brand Devices [iLifeplus]

B459SY18210JPD-FR401
B459SY18200ABP-U80R
B459SY18190JPD-FR200
B459SY18220JPD-FR200

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