Pocket Pal II™ - Pocket Pal II Kit w/352,White - AMERICAN DIAGNOSTIC CORP

Duns Number:108999095

Device Description: Pocket Pal II Kit w/352,White

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More Product Details

Catalog Number

116W1

Brand Name

Pocket Pal II™

Version/Model Number

116W1

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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"

-

For Single-Use

-

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 Details

Product Code

LRW

Product Code Name

Scissors, General, Surgical

Device Record Status

Public Device Record Key

60db43cb-b15c-4ae0-99b4-bc503a4c47ab

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

February 03, 2017

Additional Identifiers

Package DI Number

00634782587147

Quantity per Package

24

Contains DI Package

00634782085742

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case

"AMERICAN DIAGNOSTIC CORP" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2395
2 A medical device with a moderate to high risk that requires special controls. 1769