FDA UDI In Commercial Distribution 🇺🇸 United States

TwitchView™

DI: 00860298001031 · Model: Monitor v1 · BLINK DEVICE COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TwitchView™
Primary DI
00860298001031
Version / Model
Monitor v1
Company Name
BLINK DEVICE COMPANY
Labeler DUNS
105714027
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-05
Public Version
1
Public Version Date
2018-10-08
Public Version Status
New
Public Device Record Key
0f586106-5609-4909-a820-f71736f89767

Device Description

TwitchView™ utilizes advanced electromyography (EMG) to quantify a patient's depth of neuromuscular block. Providing clinicians with reliable, accurate, and real-time data to support drug dosing and reversal timing and helps prevent residual neuromuscular blockade.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KOI Stimulator, Nerve, Peripheral, Electric

GMDN Terms

Code Name
35722 Block-monitoring peripheral nerve electrical stimulation system

Identifiers

Type ID
Primary 00860298001031

Premarket Submissions

Submission Number Supplement Number
K172843 000