FDA UDI In Commercial Distribution 🇺🇸 United States

BioPlex 2200

DI: 03610520506349 · Model: SW4.2 V3 · BIO-RAD LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioPlex 2200
Primary DI
03610520506349
Version / Model
SW4.2 V3
Catalog Number
6653775A
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
4d9b3732-89f4-4519-9ce7-a9c01de8aee9

Device Description

25-OH Vitamin D Assay Protocol File CD, SW4.2_v3, US

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
MRG SYSTEM, TEST, VITAMIN D

GMDN Terms

Code Name
60922 Multiple form 25-hydroxy vitamin D IVD, kit, chemiluminescent immunoassay

Identifiers

Type ID
Primary 03610520506349

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 Each