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QC Sets and Panels: Helix Elite™
EUDAMEDFDA UDIClass B (EU MDR)
Ref [8249] QC Sets and Panels: Helix Elite™ Bacterial Vaginosis (BV) Control PanelModel 8249
Identity
- Trade Name
- QC Sets and Panels: Helix Elite™ FDA UDI
- Generic Name
- Multiple vaginitis/vaginosis-associated pathogen nucleic acid IVD, control FDA UDI
- Device Name
- QC Sets and Panels: Helix Elite™ EUDAMEDQC Sets and Panels: Helix Elite™ Molecular Standards Bacterial vaginosis (BV) Control Panel FDA UDI
- Model / Reference
- 8249 EUDAMEDFDA UDI[8249] QC Sets and Panels: Helix Elite™ Bacterial Vaginosis (BV) Control Panel EUDAMED
- Description
- QC Sets and Panels: Helix Elite™ Molecular Standards Bacterial vaginosis (BV) Control Panel FDA UDI
Identifiers
- Catalog Number
- 8249 FDA UDI
- Primary DI / UDI-DI
- 70845357043732 EUDAMEDFDA UDI
- Basic UDI-DI
- 084535708249BL EUDAMED
- FDA Product Code
- OHQ FDA UDI
- EMDN Code
- W0105080807 MULTICONSTITUENT CONTROLS - INF.IMM. EUDAMED
- GMDN Term
- Multiple vaginitis/vaginosis-associated pathogen nucleic acid IVD, control FDA UDI
Classification
- Device Class
- Class B EUDAMEDClass I FDA UDI
- Regulation Number
- 862.1660 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
Yes
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
No
FDA UDI
QC Sets and Panels: Helix Elite™ by Microbiologics Inc. — Class B — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 084535708249BL | Class B | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class B | Pending data |
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Manufacturer
- Manufacturer
- Microbiologics, INC.
- EUDAMED SRN
- US-MF-000000466
- Authorised Representative
- MediMark Europe Sarl. FR-AR-000000182
Sources (2)
- EUDAMED 1298aa1d-fa43-4d44-9d82-b364e6ba424d 61 fields · synced May 30, 2026
- FDA UDI 55c5a0fc-d0a2-4346-9254-19ad21ac3f7b 36 fields · synced May 30, 2026