Catalog Number

SBF-001D-05

Brand Name

Bipolar Forceps

Version/Model Number

SBF-001D-05

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

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

K002257,K002257

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

614fc3fa-a502-4f81-b0a4-c6322b5259fd

Public Version Date

September 27, 2021

Public Version Number

1

DI Record Publish Date

September 19, 2021

Package DI Number

00810026181153

Quantity per Package

5

Contains DI Package

00810026181184

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case