CHATTANOOGA - Storz Medical AG

Duns Number:481967776

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More Product Details

Catalog Number

-

Brand Name

CHATTANOOGA

Version/Model Number

CHATTANOOGA Intelect F-SW USA

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

P080028

Product Code Details

Product Code

NBN

Product Code Name

Generator, Shock-Wave, For Pain Relief

Device Record Status

Public Device Record Key

0bc707f3-fbb0-474e-a645-bde7dccede40

Public Version Date

July 06, 2018

Public Version Number

2

DI Record Publish Date

May 28, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"STORZ MEDICAL AG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 18
2 A medical device with a moderate to high risk that requires special controls. 11
3 A medical device with high risk that requires premarket approval 7