Catalog Number

-

Brand Name

NA

Version/Model Number

BT1000SC

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

K812292,K812292

Product Code

CAC

Product Code Name

APPARATUS, AUTOTRANSFUSION

Public Device Record Key

a97c2d97-e30f-434a-b6e0-fc094f44b983

Public Version Date

January 08, 2021

Public Version Number

4

DI Record Publish Date

June 17, 2015

Package DI Number

10673978522217

Quantity per Package

24

Contains DI Package

00673978522210

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

PK