Integra® Miltex® - Explorer, Tufts 17-23, Double-Ended, GripLite® S6 - INTEGRA LIFESCIENCES PRODUCTION CORPORATION

Duns Number:081277700

Device Description: Explorer, Tufts 17-23, Double-Ended, GripLite® S6

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

80-5303

Brand Name

Integra® Miltex®

Version/Model Number

80-5303

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 01, 2022

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)

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

EKB

Product Code Name

EXPLORER, OPERATIVE

Device Record Status

Public Device Record Key

b7264b2c-70b9-4437-b7a3-fec569fefedb

Public Version Date

July 20, 2022

Public Version Number

3

DI Record Publish Date

April 19, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INTEGRA LIFESCIENCES PRODUCTION CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 15051
2 A medical device with a moderate to high risk that requires special controls. 4286
3 A medical device with high risk that requires premarket approval 2
U Unclassified 3