Catalog Number

1001-82P

Brand Name

Scanlan® SURG-I-LOOP® PLUS with semi-sharp needle

Version/Model Number

1001-82P

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

GAE

Product Code Name

Snare, Surgical

Public Device Record Key

ad5cd627-1f00-4ed1-a7c5-b7550998a6f7

Public Version Date

May 06, 2020

Public Version Number

3

DI Record Publish Date

July 21, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-