Subdural Electrode - AD-TECH MEDICAL INSTRUMENT CORPORATION

Duns Number:174813410

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More Product Details

Catalog Number

TS12R-AP10X-0W6

Brand Name

Subdural Electrode

Version/Model Number

TS12R-AP10X-0W6

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

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)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K053363

Product Code Details

Product Code

GYC

Product Code Name

ELECTRODE, CORTICAL

Device Record Status

Public Device Record Key

09c141ca-3bc2-469c-948d-8e0379c8e86f

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 23, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AD-TECH MEDICAL INSTRUMENT CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 29
2 A medical device with a moderate to high risk that requires special controls. 796