MPK-10-R/2,0m - BIOTRONIK SE & Co. KG

Duns Number:315620229

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More Product Details

Catalog Number

353173

Brand Name

MPK-10-R/2,0m

Version/Model Number

353173

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

K201445,K212593

Product Code Details

Product Code

DRF

Product Code Name

CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING

Device Record Status

Public Device Record Key

0bd738c2-7d8c-4408-8753-b35c1723a862

Public Version Date

August 25, 2022

Public Version Number

2

DI Record Publish Date

October 22, 2021

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