AccessGUDID - DEVICE: TwitchView™ (00860298001055)

GUDID

Device Identifier (DI) Information

Brand Name: TwitchView™
Version or Model: Electrode v1
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: BLINK DEVICE COMPANY

Primary DI Number: 00860298001055
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 105714027 *Terms of Use

Device Description: Supporting infection control, TwitchView™ utilizes a single-patient use Electrode Array. With the flexibility to secure to either left or right hand in seconds, the Electrode Array is easily adopted into the pre-surgical workflow. The one-piece, auto-centering design mitigates placement errors—a common cause of intra-operative system failure and measurement inaccuracies.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
59689	Neuromuscular transmission electrode	A non-sterile electrical conductor designed to be applied to a patient's body surface, typically the forearm or ankle, to deliver stimulating electrical pulses to a motor nerve or measure electrical impulses from the nerve during neuromuscular transmission (NMT) monitoring. It is typically a disk-like electrode that is affixed to the skin with a special adhesive and a conductive gel (pre-gelled) intended to be used for neuromuscular block monitoring and nerve stimulation for brachial plexus anaesthesia. This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
KOI	Stimulator, Nerve, Peripheral, Electric

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K172843	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 18634b3f-962b-4495-a511-f5735dd1e606
Public Version Date: October 08, 2018
Public Version Number: 1
DI Record Publish Date: September 05, 2018