FDA UDI In Commercial Distribution 🇺🇸 United States

BioPlex 2200

DI: 03610520178904 · Model: SW4.3_v5 · BIO-RAD LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioPlex 2200
Primary DI
03610520178904
Version / Model
SW4.3_v5
Catalog Number
12003844
Company Name
BIO-RAD LABORATORIES, INC.
Labeler DUNS
884513334
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-09
Public Version
5
Public Version Date
2022-03-22
Public Version Status
Update
Public Device Record Key
1a8a699b-0144-4da5-8fd6-b2906a10747f

Device Description

U.S. IFU, Manual & CDs, BioPlex 2200 HIV Ag-Ab IFU, SW 4.3_v5

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
MZF Test, hiv detection

GMDN Terms

Code Name
43472 Laboratory instrument/analyser application software IVD

Identifiers

Type ID
Primary 03610520178904

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 Each