Isolibrium - Isolibrium PE - STRYKER CORPORATION

Duns Number:078470558

Device Description: Isolibrium PE

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More Product Details

Catalog Number

297300000000

Brand Name

Isolibrium

Version/Model Number

297300000000

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

-

Product Code Details

Product Code

IKZ

Product Code Name

BED, PATIENT ROTATION, POWERED

Device Record Status

Public Device Record Key

6cf5a045-d26a-4529-9e4e-4b19822d449b

Public Version Date

May 26, 2021

Public Version Number

1

DI Record Publish Date

May 18, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"STRYKER CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2188
2 A medical device with a moderate to high risk that requires special controls. 3183
U Unclassified 60