Floodlight MS Pinching Test 09341889001

GUDID 07613336193259

Roche Molecular Systems, Inc.

Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software Self-care monitoring/reporting software

Primary Device ID	07613336193259
NIH Device Record Key	86a1a988-276d-445f-9478-98067915c5d1
Commercial Distribution Status	In Commercial Distribution
Brand Name	Floodlight MS Pinching Test
Version Model Number	09341889001
Catalog Number	09341889001
Company DUNS	117676383
Company Name	Roche Molecular Systems, 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	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	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613336193259 [Primary]

FDA Product Code

GWW	Ataxiagraph

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2021-01-25
Device Publish Date	2021-01-15

On-Brand Devices [Floodlight MS Pinching Test ]

07613336193259	09341889001
07613336193242	09341862001