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QC Sets and Panels: Helix Elite™

EUDAMEDFDA UDI

Class B (EU MDR)

Ref [8219] QC Sets and Panels: Helix Elite™ Group A Streptococcus (GAS) Control PanelModel 8219

by Microbiologics, INC.

Identity

Trade Name
QC Sets and Panels: Helix Elite™ FDA UDI
Generic Name
Beta-haemolytic Group A Streptococcus nucleic acid IVD, control FDA UDI
Device Name
QC Sets and Panels: Helix Elite™ EUDAMED
QC Sets and Panels: Helix Elite™ Group A Streptococcus (GAS) Control Panel FDA UDI
Model / Reference
8219 EUDAMEDFDA UDI
[8219] QC Sets and Panels: Helix Elite™ Group A Streptococcus (GAS) Control Panel EUDAMED
Description
QC Sets and Panels: Helix Elite™ Group A Streptococcus (GAS) Control Panel FDA UDI

Identifiers

Catalog Number
8219 FDA UDI
Primary DI / UDI-DI
70845357041493 EUDAMEDFDA UDI
Basic UDI-DI
084535708219BB EUDAMED
FDA Product Code
OHQ FDA UDI
EMDN Code
W0105080801 BACTERIOLOGY CONTROLS - INF.IMM. EUDAMED
GMDN Term
Beta-haemolytic Group A Streptococcus nucleic acid IVD, control FDA UDI

Classification

Device Class
Class B EUDAMED
Class 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000000466
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 6610ce3f-64e2-4a89-bb1d-ea8033c1d199 61 fields · synced May 30, 2026
  • FDA UDI ea406158-2357-4a84-a5fc-18cc8845cb9c 36 fields · synced May 30, 2026