IDryNeedle 0.25x30 - Feeltech Co.,Ltd.

Duns Number:688432407

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More Product Details

Catalog Number

-

Brand Name

IDryNeedle 0.25x30

Version/Model Number

DN150 0.25x30

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

MQX

Product Code Name

Needle, Acupuncture, Single Use

Device Record Status

Public Device Record Key

7190119b-0530-45d9-ac39-73cfb210ea80

Public Version Date

May 24, 2021

Public Version Number

2

DI Record Publish Date

January 15, 2020

Additional Identifiers

Package DI Number

28809407787011

Quantity per Package

1000

Contains DI Package

18809407787014

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

OUTBOX

"FEELTECH CO.,LTD." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 2