IMAK RSI

GUDID 00649833103122

Wrist orthosis

Primary Device ID	00649833103122
NIH Device Record Key	ed999a4e-8e07-4c6f-944c-fd4c5b3eb18b
Commercial Distribution Status	In Commercial Distribution
Brand Name	IMAK RSI
Version Model Number	A10312
Company DUNS	091999771
Company Name	BROWNMED, INC.
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	true
RX Perscription	false
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00649833103122 [Primary]

ILH	Splint, Hand, And Components

Steralize Prior To Use	false
Device Is Sterile	false