FDA UDI Not in Commercial Distribution 🇺🇸 United States

BioPlex 2200

DI: 00847865001342 · Model: SW4.1_V2 · BIO-RAD LABORATORIES, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioPlex 2200
Primary DI
00847865001342
Version / Model
SW4.1_V2
Catalog Number
6651160H
Company Name
BIO-RAD LABORATORIES, INC.
Labeler DUNS
884513334
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-12
Public Version
3
Public Version Date
2019-11-07
Public Version Status
Update
Public Device Record Key
4a16d1fd-7dc7-4271-92c0-0dc3bfefc020
Distribution End Date
2019-09-13

Device Description

Manual & CDs, ANA Screen with MDSS IFU, SW4.1_v2

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LKO ANTI-RNP ANTIBODY, ANTIGEN AND CONTROL
LKJ ANTINUCLEAR ANTIBODY, ANTIGEN, CONTROL
LLL EXTRACTABLE ANTINUCLEAR ANTIBODY, ANTIGEN AND CONTROL
MQA ANTI-RIBOSOMAL P ANTIBODIES
LJM ANTINUCLEAR ANTIBODY (ENZYME-LABELED), ANTIGEN, CONTROLS
LRM ANTI-DNA ANTIBODY (ENZYME-LABELED), ANTIGEN, CONTROL

GMDN Terms

Code Name
54810 Multiple antinuclear antibody (ANA) screening IVD, kit, multiplex

Identifiers

Type ID
Primary 00847865001342

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 Each