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MGB Alert® Chlamydophila Pneumoniae Probe Mix ASR - 48 Reactions
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- MGB Alert® Chlamydophila Pneumoniae Probe Mix ASR - 48 Reactions FDA UDI
- Generic Name
- Chlamydia pneumoniae nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
- Device Name
- MGB Alert® Chlamydophila pneumoniae Probe is an analyte specific reagent that contains a chemically synthesized DNA oligonucleotide designed to detect the Major Outer Membrane protein gene region of Chlamydophila pneumoniae. The mix consists of one probe at 0.72 nmol per vial in a 1X TE buffer solution. The probe is labeled with fluorescein (FAM) and has an excitation wavelength maxima of 496 nm and an emission wavelength maxima of 517 nm. FDA UDI
- Model / Reference
- 800434 FDA UDI
- Description
- MGB Alert® Chlamydophila pneumoniae Probe is an analyte specific reagent that contains a chemically synthesized DNA oligonucleotide designed to detect the Major Outer Membrane protein gene region of Chlamydophila pneumoniae. The mix consists of one probe at 0.72 nmol per vial in a 1X TE buffer solution. The probe is labeled with fluorescein (FAM) and has an excitation wavelength maxima of 496 nm and an emission wavelength maxima of 517 nm. FDA UDI
Identifiers
- Catalog Number
- 800434 FDA UDI
- Primary DI / UDI-DI
- 03661540951770 FDA UDI
- FDA Product Code
- MVU FDA UDI
- GMDN Term
- Chlamydia pneumoniae 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: Chlamydia pneumoniae nucleic acid IVD, kit, nucleic acid technique (NAT)
MGB Alert® Chlamydophila Pneumoniae Probe Mix ASR - 48 Reactions by ELITechGroup MDX LLC. — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Chlamydia pneumoniae 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 e68235f0-0faf-4bb5-9cfe-57dee002f15c 36 fields · synced May 30, 2026