FDA UDI In Commercial Distribution 🇺🇸 United States

QMedix™

DI: 10850049545492 · Model: DACD104110-1-19 · Diagnostic Automation, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

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Basic Information

Brand Name
QMedix™
Primary DI
10850049545492
Version / Model
DACD104110-1-19
Catalog Number
104110-1-19
Company Name
Diagnostic Automation, Inc.
Labeler DUNS
878252071
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2025-12-24
Public Version
1
Public Version Date
2026-01-01
Public Version Status
New
Public Device Record Key
4a3de556-7653-4588-ba04-b1fabfc9f025

Device Description

QMedix™ LH Ovulation Urine RapiCard™ InstaTest

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
CEP Radioimmunoassay, Luteinizing Hormone

GMDN Terms

Code Name
54255 Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Unit of Use 00850049545495
Primary 10850049545492

Customer Contacts

Phone
8185913030

Device Sizes

Type Value Unit Text
Device Size Text, specify 25

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius