Catalog Number

SG-111-622

Brand Name

Biopsy Forceps

Version/Model Number

SG-111-622

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 04, 2019

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"

Yes

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

FCL

Product Code Name

Forceps, Biopsy, Non-Electric

Public Device Record Key

79998bfe-77dd-4279-b445-56b7ed1e1237

Public Version Date

November 05, 2019

Public Version Number

2

DI Record Publish Date

May 14, 2018

Package DI Number

10816207020751

Quantity per Package

10

Contains DI Package

00816207020754

Package Discontinue Date

November 04, 2019

Package Status

Not in Commercial Distribution

Package Type

bOX