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Helix Elite™ Molecular Standards: Inactivated Standard
EUDAMEDFDA UDIClass B (EU MDR)
Ref [HE0037N] Helix Elite™ Molecular Standards Inactivated Herpes Simplex Virus 2 Strain MSModel HE0037N
Identity
- Trade Name
- Helix Elite™ Molecular Standards: Inactivated Standard FDA UDI
- Generic Name
- Multiple Human herpesvirus nucleic acid IVD, control FDA UDI
- Device Name
- Helix Elite™ Molecular Standards: Inactivated Standard EUDAMEDHelix Elite™ Molecular Standards Inactivated Herpes Simplex Virus 2 Strain MS FDA UDI
- Model / Reference
- HE0037N EUDAMEDFDA UDI[HE0037N] Helix Elite™ Molecular Standards Inactivated Herpes Simplex Virus 2 Strain MS EUDAMED
- Description
- Helix Elite™ Molecular Standards Inactivated Herpes Simplex Virus 2 Strain MS FDA UDI
Identifiers
- Catalog Number
- HE0037N FDA UDI
- Primary DI / UDI-DI
- 10845357042115 EUDAMEDFDA UDI
- Basic UDI-DI
- 08453570HE0037NZ6 EUDAMED
- FDA Product Code
- OHQ FDA UDI
- EMDN Code
- W0105080804 OTHER VIROLOGY CONTROLS - INF.IMM. EUDAMED
- GMDN Term
- Multiple Human herpesvirus 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
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
No
FDA UDI
Helix Elite™ Molecular Standards: Inactivated Standard by Microbiologics Inc. — Class B — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID
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 | 08453570HE0037NZ6 | 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 a69e6eca-e28f-43e3-86bb-7efe07913f64 61 fields · synced May 31, 2026
- FDA UDI ff32a099-33ed-491c-8342-0599bdca64b8 36 fields · synced May 30, 2026