Collimator AL02 II eL - Siemens Healthcare GmbH

Duns Number:313217003

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More Product Details

Catalog Number

-

Brand Name

Collimator AL02 II eL

Version/Model Number

10092614

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

-

Product Code Details

Product Code

KPW

Product Code Name

Device, beam limiting, x-ray, diagnostic

Device Record Status

Public Device Record Key

8b02821a-9df7-4e77-af6e-c11701c2b959

Public Version Date

November 18, 2021

Public Version Number

4

DI Record Publish Date

October 23, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SIEMENS HEALTHCARE GMBH" 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. 478
3 A medical device with high risk that requires premarket approval 1