RONDEX CPR REDI-SHIELD (Made in USA) in key ring case with gloves - The RONDEX CPR REDI-SHIELD model #9850-G comes - RONDEX PRODUCTS, INCORPORATED

Duns Number:021435706

Device Description: The RONDEX CPR REDI-SHIELD model #9850-G comes in a case with a key ring and gloves. It The RONDEX CPR REDI-SHIELD model #9850-G comes in a case with a key ring and gloves. It is a mouth-to-mask barrier device used to help a rescuer avoid direct contact with the patient when doing resuscitation. Barrier surface area (6" X 6") helps isolate the rescuer from the patient. The barrier material is attached to a short bite block containing one (1) silicone valve which helps to isolate the patient's breath from the rescuer. The bite block helps to keep the barrier positioned correctly while keeping the patient's mouth open. This makes ventilation much easier when doing the head tilt/chin lift procedure. The short bite block, 1/2" in length, reduces the risk of pushing the patient's tongue back and does not require a prescription. This device is for emergency use only and should only be used by persons properly trained in CPR and in the use of this device. REDI-SHIELD(TM) of Rondex MADE IN USA.

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More Product Details

Catalog Number

9850-G

Brand Name

RONDEX CPR REDI-SHIELD (Made in USA) in key ring case with gloves

Version/Model Number

9850-G (packaged in key ring case)

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

LYM

Product Code Name

Device, Cpr Assist

Device Record Status

Public Device Record Key

36a28c52-299d-400e-bc87-320447a2d6f0

Public Version Date

September 11, 2020

Public Version Number

1

DI Record Publish Date

September 03, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"RONDEX PRODUCTS, INCORPORATED" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 7
U Unclassified 22