George King Prekallikrein Deficient Plasma - George King Prekallikrein Deficient plasma is - GEORGE KING BIO-MEDICAL, INC

Duns Number:066761271

Device Description: George King Prekallikrein Deficient plasma is fresh frozen citrated human plasma derived f George King Prekallikrein Deficient plasma is fresh frozen citrated human plasma derived from congenital Prekallikrein Deficient donors

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More Product Details

Catalog Number

-

Brand Name

George King Prekallikrein Deficient Plasma

Version/Model Number

1700-1.0

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

-

Product Code Details

Product Code

GGC

Product Code Name

Control, Plasma, Abnormal

Device Record Status

Public Device Record Key

5735d0e4-841d-4768-a26d-4519e048d405

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

August 18, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"GEORGE KING BIO-MEDICAL, INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 120