FDA UDI In Commercial Distribution 🇺🇸 United States

VITEK® 2 NH

DI: 03573026529710 · Model: VITEK® 2 NH · BIOMERIEUX , INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VITEK® 2 NH
Primary DI
03573026529710
Version / Model
VITEK® 2 NH
Company Name
BIOMERIEUX , INC.
Labeler DUNS
086785110
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-02
Public Version
2
Public Version Date
2022-05-10
Public Version Status
Update
Public Device Record Key
151f682a-1f73-4d75-8166-385fa23c2e58

Device Description

The VITEK® 2 NH Identification Card is intended for use with the VITEK 2 Systems for ID of clinically important Neisseria, Haemophilus and other fastidious GN bacteria

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JST KIT, FASTIDIOUS ORGANISMS

GMDN Terms

Code Name
50423 Multiple Haemophilus/Neisseria bacteria species culture isolate identification IVD, kit

Identifiers

Type ID
Package 03573026144357
Primary 03573026529710

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius