Catalog Number

BL-0150

Brand Name

N/A

Version/Model Number

BL-0150

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"

Yes

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

KDC

Product Code Name

Instrument, Surgical, Disposable

Public Device Record Key

47a3609e-bb51-41c6-bbf7-936eebeba94e

Public Version Date

August 23, 2021

Public Version Number

8

DI Record Publish Date

August 17, 2016

Package DI Number

20385640000653

Quantity per Package

12

Contains DI Package

00385640000659

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box