Hu-Friedy - P24GSPX/PFIWDS1MKX Periosteal Black Line - HU-FRIEDY MFG. CO., LLC

Duns Number:005085972

Device Description: P24GSPX/PFIWDS1MKX Periosteal Black Line

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More Product Details

Catalog Number

PFI57027

Brand Name

Hu-Friedy

Version/Model Number

PFI57027

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

EMJ

Product Code Name

ELEVATOR, SURGICAL, DENTAL

Device Record Status

Public Device Record Key

ba885cfd-5ffb-4add-8456-3ab2f67492c4

Public Version Date

May 24, 2021

Public Version Number

1

DI Record Publish Date

May 14, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HU-FRIEDY MFG. CO., LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 7436
2 A medical device with a moderate to high risk that requires special controls. 238