Alinity - Alinity i ROMA - Abbott GmbH

Duns Number:315786293

Device Description: Alinity i ROMA

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More Product Details

Catalog Number

03R7521

Brand Name

Alinity

Version/Model Number

03R7521

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K151502

Product Code Details

Product Code

ONX

Product Code Name

Ovarian adnexal mass assessment score test system

Device Record Status

Public Device Record Key

0768e505-dfff-489e-8680-2c7a41d938c7

Public Version Date

August 18, 2020

Public Version Number

1

DI Record Publish Date

August 10, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ABBOTT GMBH" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 347
2 A medical device with a moderate to high risk that requires special controls. 185
3 A medical device with high risk that requires premarket approval 13