Actherm

GUDID 06972325560016

Intermittent electronic patient thermometer

Primary Device ID	06972325560016
NIH Device Record Key	0bb725ba-605e-4347-9ea3-f0b0e2ddc26c
Commercial Distribution Status	In Commercial Distribution
Brand Name	Actherm
Version Model Number	2030
Company DUNS	544571542
Company Name	Dongguan Actherm Medical Corp.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	06972325560016 [Primary]
GS1	06972325560320 [Package] Package: [10 Units] In Commercial Distribution
GS1	06972325560535 [Package] Package: [200 Units] In Commercial Distribution
GS1	06972325560740 [Package] Package: [100 Units] In Commercial Distribution
GS1	06972325560993 [Package] Package: [600 Units] In Commercial Distribution

FLL	Thermometer, Electronic, Clinical

Steralize Prior To Use	false
Device Is Sterile	false

Mark Image Registration \| Serial	Company Trademark Application Date
ACTHERM 76547996 2874112 Live/Registered	ACTHERM INC. 2003-09-29
ACTHERM 76547995 2937341 Dead/Cancelled	ACTHERM INC. 2003-09-29