Catalog Number

32028107

Brand Name

Vermed

Version/Model Number

SHRP12 GAL SHARPS W/PORT/DUO LID

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"

Yes

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K071517,K071517,K071517

Product Code

MMK

Product Code Name

Container, Sharps

Public Device Record Key

cba6d8b8-a957-49a8-acae-3eeb7a8fc850

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 24, 2017

Package DI Number

70009336006457

Quantity per Package

16

Contains DI Package

50009336006453

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Pallet