FDA UDI Not in Commercial Distribution 🇺🇸 United States

BioPlex 2200

DI: 00847865003186 · Model: SW4_ V3 · BIO-RAD LABORATORIES, INC.
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioPlex 2200
Primary DI
00847865003186
Version / Model
SW4_ V3
Catalog Number
6653870C
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
2021-07-29
Public Version Status
Update
Public Device Record Key
d56ccd61-1cc6-4b0b-8eef-1a1d19b2af81
Distribution End Date
2021-07-06

Device Description

Rubella & CMV Assay Protocol File CD, SW4_v3

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
LFZ ENZYME LINKED IMMUNOABSORBENT ASSAY, CYTOMEGALOVIRUS
LKQ ANTIBODY IGM,IF, CYTOMEGALOVIRUS VIRUS
LFX ENZYME LINKED IMMUNOABSORBENT ASSAY, RUBELLA

GMDN Terms

Code Name
49725 Cytomegalovirus (CMV) immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay
50269 Rubella virus immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay

Identifiers

Type ID
Primary 00847865003186

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 Each