Arrive™ Braided Transseptal Sheath - Braided Transseptal Sheath, 10F - Oscor Inc.

Duns Number:101835833

Device Description: Braided Transseptal Sheath, 10F

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More Product Details

Catalog Number

990061-120

Brand Name

Arrive™ Braided Transseptal Sheath

Version/Model Number

990061-120

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

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

K101497

Product Code Details

Product Code

DYB

Product Code Name

INTRODUCER, CATHETER

Device Record Status

Public Device Record Key

22b6d212-3427-4059-81b5-8b92a1922212

Public Version Date

December 22, 2021

Public Version Number

7

DI Record Publish Date

November 21, 2017

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"OSCOR INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 592
3 A medical device with high risk that requires premarket approval 16