FDA UDI In Commercial Distribution 🇺🇸 United States

BioPlex 2200

DI: 00847865002172 · Model: SW4.1_V2 · BIO-RAD LABORATORIES, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
BioPlex 2200
Primary DI
00847865002172
Version / Model
SW4.1_V2
Catalog Number
6653360F
Company Name
BIO-RAD LABORATORIES, INC.
Labeler DUNS
884513334
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-12
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9b957d6f-3c22-4bde-b344-994624b8d3a0

Device Description

Manual & CDs, HSV-1 & HSV-2 IgG 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
MYF Enzyme linked immunosorbent assay, herpes simplex virus, hsv-2
MXJ Enzyme linked immunosorbent assay, herpes simplex virus, hsv-1

GMDN Terms

Code Name
49544 Herpes simplex virus 1 & 2 (HSV1 & 2) immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay

Identifiers

Type ID
Primary 00847865002172

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 Each