Progensa - Hologic, Inc.

Duns Number:050579217

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More Product Details

Catalog Number

302002C

Brand Name

Progensa

Version/Model Number

ASSAY FLUIDS KIT

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

P100033

Product Code Details

Product Code

LSL

Product Code Name

DNA-REAGENTS, NEISSERIA

Device Record Status

Public Device Record Key

be8d4dd6-65fd-44e4-baa3-f5e7a884a6d9

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 17, 2014

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HOLOGIC, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 130
2 A medical device with a moderate to high risk that requires special controls. 311
3 A medical device with high risk that requires premarket approval 96