FDA UDI In Commercial Distribution 🇺🇸 United States

QIAstat-Dx® Meningitis/Encephalitis (ME) Panel

DI: 04053228043850 · Model: V2 · QIAGEN GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
QIAstat-Dx® Meningitis/Encephalitis (ME) Panel
Primary DI
04053228043850
Version / Model
V2
Catalog Number
691621
Company Name
QIAGEN GmbH
Labeler DUNS
317103745
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-31
Public Version
4
Public Version Date
2026-02-05
Public Version Status
Update
Public Device Record Key
7508579d-a0c7-45be-a31d-2f29058f0b21

Device Description

IVD kit containing 6 tests

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
Yes
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
PLO Meningitis/Encephalitis Pathogen Multiplex Nucleic Acid Detection System

GMDN Terms

Code Name
61043 Multiple-type meningitis pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)

Identifiers

Type ID
Primary 04053228043850
Package 14053228043857

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Room temperature