dS MSK S 1.5T - The Device is designed to be used in conjunction - Philips Healthcare (Suzhou) Co., Ltd.

Duns Number:421265537

Device Description: The Device is designed to be used in conjunction with MR Scanner to produce diagnostic ima The Device is designed to be used in conjunction with MR Scanner to produce diagnostic images of the anatomy of interest that can be interpreted by a trained physician.

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More Product Details

Catalog Number

-

Brand Name

dS MSK S 1.5T

Version/Model Number

45980168200X

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

K212864

Product Code Details

Product Code

MOS

Product Code Name

Coil, Magnetic Resonance, Specialty

Device Record Status

Public Device Record Key

ba3a95ac-9894-4c60-983f-d028909de64e

Public Version Date

April 25, 2022

Public Version Number

1

DI Record Publish Date

April 17, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"PHILIPS HEALTHCARE (SUZHOU) CO., LTD." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 10