Catalog Number

AN-1050

Brand Name

METRO-PACIFICA

Version/Model Number

AN-1050

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

LZC

Product Code Name

Patient examination glove, specialty

Public Device Record Key

a072a427-774b-4020-a58d-8297a5899409

Public Version Date

June 19, 2020

Public Version Number

2

DI Record Publish Date

April 26, 2019

Package DI Number

00609626063279

Quantity per Package

10

Contains DI Package

00609626063286

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE