Curaplex - Curaplex Supraglottic Airway Kit, King LTS-D, - BOUND TREE MEDICAL, LLC

Duns Number:070556204

Device Description: Curaplex Supraglottic Airway Kit, King LTS-D, Size 2, 12-25 kg

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More Product Details

Catalog Number

477-KLTSD412

Brand Name

Curaplex

Version/Model Number

477-KLTSD412

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

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

CAE

Product Code Name

AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

Device Record Status

Public Device Record Key

a81dea59-0a83-4cd0-86a4-c323883cce3c

Public Version Date

August 16, 2022

Public Version Number

5

DI Record Publish Date

December 27, 2016

Additional Identifiers

Package DI Number

00810094570354

Quantity per Package

30

Contains DI Package

00817617020532

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS

"BOUND TREE MEDICAL, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 471
2 A medical device with a moderate to high risk that requires special controls. 540
3 A medical device with high risk that requires premarket approval 3
U Unclassified 1