Atellica IM TnI-Ultra - TnI-Ultra Atellica IM - RGT 500T - Siemens Healthcare Diagnostics Inc.

Duns Number:064608573

Device Description: TnI-Ultra Atellica IM - RGT 500T

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More Product Details

Catalog Number

10995697

Brand Name

Atellica IM TnI-Ultra

Version/Model Number

10995697

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

K053020

Product Code Details

Product Code

MMI

Product Code Name

IMMUNOASSAY METHOD, TROPONIN SUBUNIT

Device Record Status

Public Device Record Key

4d3f1b28-7d96-4bfa-98f6-f6e2332c7401

Public Version Date

November 18, 2021

Public Version Number

5

DI Record Publish Date

February 06, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SIEMENS HEALTHCARE DIAGNOSTICS INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 363
2 A medical device with a moderate to high risk that requires special controls. 829
3 A medical device with high risk that requires premarket approval 57
U Unclassified 7