Charder - CHARDER ELECTRONIC CO., LTD.

Duns Number:656102035

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More Product Details

Catalog Number

-

Brand Name

Charder

Version/Model Number

MS3801

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

-

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

INF

Product Code Name

Scale, Platform, Wheelchair

Device Record Status

Public Device Record Key

eb306bd0-4096-41b4-9396-753f92fbadc0

Public Version Date

December 09, 2019

Public Version Number

1

DI Record Publish Date

November 30, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CHARDER ELECTRONIC CO., LTD." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 110
2 A medical device with a moderate to high risk that requires special controls. 35