Sentinel Chest Trauma Kit - SENTINEL CHEST TRAUMA KIT2 ea - Sentinel Dual - Safeguard US Operating, LLC

Duns Number:118492643

Device Description: SENTINEL CHEST TRAUMA KIT2 ea - Sentinel Dual vent Chest seals with Sentinel 10x extreme s SENTINEL CHEST TRAUMA KIT2 ea - Sentinel Dual vent Chest seals with Sentinel 10x extreme strength adhesive1 ea - Dart sterile, 14 gauge x 3.25", needle / catheter for chest decompression1 ea - Dart Target 1 ea - wipe

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More Product Details

Catalog Number

20-510

Brand Name

Sentinel Chest Trauma Kit

Version/Model Number

05

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

Yes

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

GAA

Product Code Name

Needle, Aspiration And Injection, Disposable

Device Record Status

Public Device Record Key

e49a937b-296c-443d-87cf-294a8a24f0f9

Public Version Date

August 26, 2022

Public Version Number

1

DI Record Publish Date

August 18, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SAFEGUARD US OPERATING, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 217
2 A medical device with a moderate to high risk that requires special controls. 48