Iforia 7 HF-T - BIOTRONIK SE & Co. KG

Duns Number:315620229

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More Product Details

Catalog Number

390051

Brand Name

Iforia 7 HF-T

Version/Model Number

390051

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 23, 2021

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

NIK

Product Code Name

Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)

Device Record Status

Public Device Record Key

cad023f2-1c75-435c-b108-8b29153f3547

Public Version Date

August 24, 2021

Public Version Number

6

DI Record Publish Date

August 07, 2014

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BIOTRONIK SE & CO. KG" 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. 97
3 A medical device with high risk that requires premarket approval 402