MiniArc - MiniArc - ENDO PHARMACEUTICALS INC.

Duns Number:178074951

Device Description: MiniArc

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More Product Details

Catalog Number

720046-01

Brand Name

MiniArc

Version/Model Number

720046-01

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 31, 2016

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

Yes

Prescription Use (Rx)

Yes

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

PAH

Product Code Name

Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-Sling

Device Record Status

Public Device Record Key

8f653809-9b25-49a9-b50b-4e1f2ea6fdb4

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

October 24, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ENDO PHARMACEUTICALS INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3
2 A medical device with a moderate to high risk that requires special controls. 15
3 A medical device with high risk that requires premarket approval 2