Catalog Number

-

Brand Name

SteriLance Neoheel Heel Incision Safety Lancet

Version/Model Number

05-102030

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FMK

Product Code Name

Lancet, Blood

Public Device Record Key

a9fa7e88-8dbb-4586-9e33-e6cbc483c900

Public Version Date

December 29, 2020

Public Version Number

1

DI Record Publish Date

December 21, 2020

Package DI Number

36945630109042

Quantity per Package

200

Contains DI Package

16945630109048

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE