BD BBL™ Sensi-Disc™ Metronidazole - 80 µg - BD BBL™ Sensi-Disc™ Metronidazole - 80 µg - BECTON, DICKINSON AND COMPANY

Duns Number:122561087

Device Description: BD BBL™ Sensi-Disc™ Metronidazole - 80 µg

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More Product Details

Catalog Number

231605

Brand Name

BD BBL™ Sensi-Disc™ Metronidazole - 80 µg

Version/Model Number

231605

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

-

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

K813387,K813387

Product Code Details

Product Code

JTN

Product Code Name

SUSCEPTIBILITY TEST DISCS, ANTIMICROBIAL

Device Record Status

Public Device Record Key

8d9580a0-c586-4d18-a19b-b0327d5a0c06

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 03, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BECTON, DICKINSON AND COMPANY" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 611
2 A medical device with a moderate to high risk that requires special controls. 614
3 A medical device with high risk that requires premarket approval 36
U Unclassified 4