Res-Q-Vac - REPL FSP SOFT 10FR 35/14 NS - REPRO MED SYSTEMS, INC.

Duns Number:048403299

Device Description: REPL FSP SOFT 10FR 35/14 NS

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More Product Details

Catalog Number

R1F1S110N

Brand Name

Res-Q-Vac

Version/Model Number

R1F1S110N

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K894299

Product Code Details

Product Code

BSY

Product Code Name

CATHETERS, SUCTION, TRACHEOBRONCHIAL

Device Record Status

Public Device Record Key

89fc7710-a730-41a3-8ead-c7a7a081a334

Public Version Date

August 23, 2018

Public Version Number

4

DI Record Publish Date

August 19, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"REPRO MED SYSTEMS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 201
2 A medical device with a moderate to high risk that requires special controls. 99