Moxa.Bx.BamL

GUDID 14897076721822

Moxibustion container

Primary Device ID	14897076721822
NIH Device Record Key	884ce4e7-7569-4a31-b506-822390c73b08
Commercial Distribution Status	In Commercial Distribution
Brand Name	Moxa.Bx.BamL
Version Model Number	GY5338
Company DUNS	663211978
Company Name	TENS PLUS INDUSTRIAL COMPANY
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	14897076721822 [Primary]

KNM	Device, Pressure Applying

Steralize Prior To Use	false
Device Is Sterile	false