GEN4 PLUS, RESPONDER 5, ENHANCED - GEN4 PLUS, RESPONDER 5, ENHANCED - CURBELL MEDICAL PRODUCTS, INC.

Duns Number:796452311

Device Description: GEN4 PLUS, RESPONDER 5, ENHANCED

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More Product Details

Catalog Number

27760

Brand Name

GEN4 PLUS, RESPONDER 5, ENHANCED

Version/Model Number

5C410U-10161001A

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

-

Product Code Details

Product Code

ILQ

Product Code Name

System, Communication, Powered

Device Record Status

Public Device Record Key

dd4834f3-87bd-429e-9284-a2f6b7005131

Public Version Date

June 23, 2022

Public Version Number

1

DI Record Publish Date

June 15, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CURBELL MEDICAL PRODUCTS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 478
2 A medical device with a moderate to high risk that requires special controls. 8062