Identity
- Trade Name
- MGB Alert® hMPV Probe Mix ASR - 48 Reactions FDA UDI
- Generic Name
- Human metapneumovirus (hMPV) nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
- Device Name
- "MGB Alert® hMPV Probe Mix is an analyte specific reagent that contains a chemically synthesized DNA oligonucleotide designed to detect nucleic acid sequences from hMPV (human Metapneumovirus). The mix consists of one probe at 0.56 nmol of probe per vial in a 1X TE buffer solution. The probe is labeled with 6-carboxyfluorescein and has an excitation wavelength maxima of 492 nm and an emission wavelength maxima of 516 nm" FDA UDI
- Model / Reference
- 800307 FDA UDI
- Description
- "MGB Alert® hMPV Probe Mix is an analyte specific reagent that contains a chemically synthesized DNA oligonucleotide designed to detect nucleic acid sequences from hMPV (human Metapneumovirus). The mix consists of one probe at 0.56 nmol of probe per vial in a 1X TE buffer solution. The probe is labeled with 6-carboxyfluorescein and has an excitation wavelength maxima of 492 nm and an emission wavelength maxima of 516 nm" FDA UDI
Identifiers
- Catalog Number
- 800307 FDA UDI
- Primary DI / UDI-DI
- 03661540951268 FDA UDI
- FDA Product Code
- MVU FDA UDI
- GMDN Term
- Human metapneumovirus (hMPV) nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.4020 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Human metapneumovirus (hMPV) nucleic acid IVD, kit, nucleic acid technique (NAT)
MGB Alert® hMPV Probe Mix ASR - 48 Reactions by ELITechGroup MDX LLC. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Human metapneumovirus (hMPV) nucleic acid IVD, kit, nucleic acid technique (NAT).
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- ELITechGroup MDX LLC.
Sources (1)
- FDA UDI ec80fdb8-c78f-44a6-b14b-4f551e6421c7 36 fields · synced May 30, 2026