Sinrel

GUDID 16978146200091

Analgesic transcutaneous electrical nerve stimulation system

Primary Device ID	16978146200091
NIH Device Record Key	319948f7-c4ac-45ae-ba8a-29fd068d0120
Commercial Distribution Status	In Commercial Distribution
Brand Name	Sinrel
Version Model Number	TENS XS PRO
Company DUNS	618769254
Company Name	SHENZHEN SINREL TECH LTD
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	false
Serial Number	false
Manufacturing Date	true
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	true

Device Issuing Agency	Device ID
GS1	06978146200094 [Primary]
GS1	16978146200091 [Package] Contains: 06978146200094 Package: [32 Units] In Commercial Distribution
GS1	26978146200098 [Package] Contains: 06978146200094 Package: [36 Units] In Commercial Distribution
GS1	36978146200095 [Package] Contains: 06978146200094 Package: [48 Units] In Commercial Distribution

NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter

Steralize Prior To Use	false
Device Is Sterile	false