LW MULTI-LINK,5LEAD,Slw,PINCH,29",BL - LW MULTI-LINK,5LEAD,Slw,PINCH,29",BL - CURBELL MEDICAL PRODUCTS, INC.

Duns Number:796452311

Device Description: LW MULTI-LINK,5LEAD,Slw,PINCH,29",BL

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More Product Details

Catalog Number

8998

Brand Name

LW MULTI-LINK,5LEAD,Slw,PINCH,29",BL

Version/Model Number

LDW-05BD-29BL-0000

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 24, 2017

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Unsafe

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K081762

Product Code Details

Product Code

DSA

Product Code Name

Cable, Transducer And Electrode, Patient, (Including Connector)

Device Record Status

Public Device Record Key

39a49ac6-cbee-4db6-a15f-2914d50470f5

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 24, 2016

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