Identity
- Trade Name
- MGB Alert® Parvovirus Probe Mix ASR - 48 Reactions FDA UDI
- Generic Name
- Parvovirus B19 nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
- Device Name
- "MGB Alert® Parvovirus B19 Probe is an analyte specific reagent that contains a chemically synthesized DNA oligonucleotide designed to detect the VP1 Capsid Protein (VP1u) gene region of Parvovirus B19. The mix consists of one probe at 0.72 nmol per vial in a 1X TE buffer solution. The probe is labeled with 6-carboxyfluorescein and has an excitation wavelength maxima of 496 nm and an emission wavelength maxima of 517 nm." FDA UDI
- Model / Reference
- M800683 FDA UDI
- Description
- "MGB Alert® Parvovirus B19 Probe is an analyte specific reagent that contains a chemically synthesized DNA oligonucleotide designed to detect the VP1 Capsid Protein (VP1u) gene region of Parvovirus B19. The mix consists of one probe at 0.72 nmol per vial in a 1X TE buffer solution. The probe is labeled with 6-carboxyfluorescein and has an excitation wavelength maxima of 496 nm and an emission wavelength maxima of 517 nm." FDA UDI
Identifiers
- Catalog Number
- M800683 FDA UDI
- Primary DI / UDI-DI
- 03661540951183 FDA UDI
- FDA Product Code
- MVU FDA UDI
- GMDN Term
- Parvovirus B19 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: Parvovirus B19 nucleic acid IVD, kit, nucleic acid technique (NAT)
MGB Alert® Parvovirus 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 Parvovirus B19 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 186f6518-9007-49c0-92e9-8fca67c8e85f 35 fields · synced May 30, 2026