FDA UDI In Commercial Distribution 🇺🇸 United States

BioPlex 2200

DI: 00847865012980 · Model: SW4.1V1 · BIO-RAD LABORATORIES, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioPlex 2200
Primary DI
00847865012980
Version / Model
SW4.1V1
Catalog Number
6652065B
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
4cd37cfa-8327-4b2c-9edf-d7ca09816634

Device Description

Manual & CDs, APLS IgM IFU, SW4.1_v1

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
MID SYSTEM, TEST, ANTICARDIOLIPIN IMMUNOLOGICAL
MSV System,test,antibodies,b2 - glycoprotein i (b2 - gpi)

GMDN Terms

Code Name
55086 Phospholipid antibody IVD, kit, multiplex

Identifiers

Type ID
Primary 00847865012980

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 Each