FDA UDI In Commercial Distribution 🇺🇸 United States

QMedix™

DI: 00850054026798 · Model: DACD 351010 · Diagnostic Automation, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
QMedix™
Primary DI
00850054026798
Version / Model
DACD 351010
Catalog Number
351010
Company Name
Diagnostic Automation, Inc.
Labeler DUNS
878252071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-14
Public Version
1
Public Version Date
2024-11-22
Public Version Status
New
Public Device Record Key
56f71457-64f8-41a9-b303-d161851c53ff

Device Description

QMedix™ FTA-ABS (Syphilis) IFA Kit 10x10 wells A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of total antibodies to Treponema pallidum in a clinical specimen using a fluorescent immunoassay method. The assay is designed to detect infection with Treponema pallidum, the bacteria associated with syphilis.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GMS Anti-Human Globulin, Fta-Abs Test

GMDN Terms

Code Name
51799 Treponema pallidum total antibody IVD, kit, fluorescent immunoassay

Identifiers

Type ID
Primary 00850054026798

Customer Contacts

Phone
8185913030

Device Sizes

Type Value Unit Text
Device Size Text, specify 10X10 WELLS

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius