EsFlow LV A2 Syringe - Spident Co., Ltd.

Duns Number:689370711

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More Product Details

Catalog Number

101-0902

Brand Name

EsFlow LV A2 Syringe

Version/Model Number

101-0902

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 25, 2021

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

-

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

K120768,K120768

Product Code Details

Product Code

EBF

Product Code Name

Material, Tooth Shade, Resin

Device Record Status

Public Device Record Key

a2b24447-f5e0-4c35-864c-b583d08ea201

Public Version Date

January 26, 2021

Public Version Number

2

DI Record Publish Date

August 23, 2018

Additional Identifiers

Package DI Number

20200623170027

Quantity per Package

30

Contains DI Package

08809262954630

Package Discontinue Date

January 25, 2021

Package Status

Not in Commercial Distribution

Package Type

-

"SPIDENT 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. 6