D3 Fastpoint - Re-Suspension Buffer - DIAGNOSTIC HYBRIDS, INC.

Duns Number:117359612

Device Description: Re-Suspension Buffer

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More Product Details

Catalog Number

01-122006

Brand Name

D3 Fastpoint

Version/Model Number

01-122006

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

K091171

Product Code Details

Product Code

GNS

Product Code Name

ANTISERA, HAI, INFLUENZA VIRUS A, B, C

Device Record Status

Public Device Record Key

0661111a-766e-42ff-bbc8-6e8390b21162

Public Version Date

March 15, 2019

Public Version Number

1

DI Record Publish Date

March 07, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"DIAGNOSTIC HYBRIDS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 549
2 A medical device with a moderate to high risk that requires special controls. 68