
Product data
| Category: | Respiratory Combo Test |
| Manufacturer: | parahealth |
| SKU: | PD-006 |
| EAN: | 4262567180014 |
| Best before: | 16.04.2028 |
| Test method: | Point-of-care test,Test für die professionelle Anwendung,Schnelltest (RDT) |
| Sample type: | Swab |
| IFU languages: | ENDEFRESITNL |
parahealth diagnostics 12-in-1 Respiratory Multitest
Benefits:
- Multi-pathogen detection (12 tests in 1)
- Result in approx. 10 minutes
- High sensitivity and specificity
- Co-infection detection across 6 windows
- Simple nasal swab collection
- CE certified for professional IVD use
- No laboratory required
- IFU available in 6 EU languages (EN/DE/FR/ES/IT/NL)
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Description
parahealth diagnostics 12-in-1 Respiratory Pathogens Antigen Rapid Test — The Most Comprehensive Rapid Panel Available
The parahealth diagnostics 12-in-1 Respiratory Multitest identifies 12 respiratory pathogens from a single nasal swab in just 10 minutes — more than any other rapid antigen test on the market. One test card, one sample, one extraction: COVID-19, Influenza A, Influenza B, RSV, Adenovirus, Mycoplasma pneumoniae, Human Metapneumovirus, Rhinovirus, Parainfluenza 1/3, Parainfluenza 2, Streptococcus pneumoniae, and Legionella pneumophila. CE-certified for professional use. Designed for clinics, hospitals, pharmacies, and occupational health services that need actionable differential diagnosis at the point of care — not just a yes/no answer for one or two pathogens.
12 Pathogens — Far Beyond the Standard 4-in-1 Combo Test
Standard combo tests cover COVID-19, Flu A/B, and RSV. The parahealth 12-in-1 goes eight pathogens further — adding Adenovirus, Mycoplasma pneumoniae, Human Metapneumovirus (HMPV), Rhinovirus, Parainfluenza virus 1/3 and 2, Streptococcus pneumoniae, and Legionella pneumophila. These are not rare findings: Mycoplasma pneumoniae is one of the most common causes of atypical pneumonia in children and young adults. Rhinovirus and HMPV together account for a significant share of respiratory infections year-round. And Legionella — traditionally requiring urine antigen or culture testing — is now detectable at the point of care from a simple nasal swab. The 12-in-1 panel turns a rapid test from a screening tool into a genuine diagnostic instrument.
One Swab, Six Windows, Twelve Answers — Co-Infections Included
The test card features six dual-detection windows: COV/MP, RSV/ADV, Flu A/Flu B, HMPV/RhV, PIV1/3/PIV2, and SP/LP. Each window screens for two pathogens simultaneously with clearly marked result lines. Critically, the test can identify co-infections across all windows — if a patient carries both Influenza A and RSV, both will show positive. This capability is essential for clinical decision-making: co-infections are common, change treatment protocols, and are invisible to single-pathogen tests.
Clinical Performance — Over 94% Sensitivity Across All 12 Targets
Every pathogen on the panel has been validated against RT-PCR as the reference method in a study of 851 samples. Influenza A achieves 97.36% PPA (positive percent agreement), COVID-19 reaches 97.00%, Influenza B 96.62%, and RSV 94.96%. Even the less common targets — Legionella, Parainfluenza, HMPV, Rhinovirus — consistently exceed 94% PPA. Cross-reactivity testing against more than 40 respiratory pathogens at 1.0 × 10⁶ copies/mL returned zero false positives. Interference testing with 26 common medications, nasal sprays, and endogenous substances confirmed no impact on results.
10-Minute Results — Fast Enough for the Consultation
Standard nasal swab from both nostrils, extraction in the supplied buffer tube, 3 drops onto the test card, results in 10 minutes. No laboratory equipment, no electricity, no specialised training beyond standard point-of-care procedures. The test is designed for the workflow of a busy GP practice, emergency department, or pharmacy testing station — results are available before the patient leaves the room. The compact single-card format means no multiple test kits, no multiple swabs, no multiple extractions. One sample answers twelve questions.
Bulk Orders for Clinics, Hospitals & Pharmacies — Direct from parahealth
The parahealth diagnostics 12-in-1 Respiratory Multitest is a parahealth own-brand product — you are buying directly from the brand. No middlemen, competitive pricing, guaranteed availability, and dedicated B2B support. Ideal stock item for GP practices, paediatric clinics, hospital emergency departments, pharmacy testing services, occupational health providers, and long-term care facilities managing respiratory seasons. Check the volume discount tiers on this page for your best price per test. Fast shipping across Europe from parahealth — your trusted partner for diagnostic supplies.
Product data
| Category: | Respiratory Combo Test |
| Manufacturer: | parahealth |
| SKU: | PD-006 |
| EAN: | 4262567180014 |
| Best before: | 16.04.2028 |
| Test method: | Point-of-care test,Test für die professionelle Anwendung,Schnelltest (RDT) |
| Sample type: | Swab |
| IFU languages: | ENDEFRESITNL |
Regulatory notices
- CE-certified in-vitro diagnostic (IVD)
- Only for business customers or medical professionals
- For single use only
- Read instructions carefully before use
- Store at room temperature (2-30 degC)
- Please note that the product you have selected is subject to a limitation of the right of return according to Sec. 312g para. 2 no. 3 BGB. As this product is a medical device, returns are excluded for hygiene reasons.
Sales inquiry / B2B
Interested in bulk orders or reseller pricing? Contact us – we will get back to you as soon as possible.
Or email us directly at sales@parahealth.de
Data sheets & Downloads
Frequently asked questions about this product
Which 12 pathogens does this rapid test detect?
The 12-in-1 panel detects COVID-19 (SARS-CoV-2), Influenza A, Influenza B, RSV, Adenovirus, Mycoplasma pneumoniae, Human Metapneumovirus (HMPV), Rhinovirus, Parainfluenza virus 1/3, Parainfluenza virus 2, Streptococcus pneumoniae, and Legionella pneumophila — all from a single nasal swab in 10 minutes.
How accurate is the 12-in-1 respiratory test compared to RT-PCR?
The test was validated against RT-PCR in a study of 851 samples. Influenza A reaches 97.36% positive percent agreement (PPA), COVID-19 97.00%, Influenza B 96.62%, RSV 94.96%. All eight remaining pathogens (Adenovirus, Mycoplasma, Parainfluenza 1/3 and 2, Streptococcus pneumoniae, HMPV, Rhinovirus, Legionella) consistently exceed 94% PPA. Specificity (NPA) ranges between 98.7% and 99.7% across all 12 targets.
Can the test identify co-infections?
Yes. The test card has six dual-detection windows (COV/MP, RSV/ADV, Flu A/Flu B, HMPV/RhV, PIV1/3/PIV2, SP/LP). If a patient carries more than one infection — for example Influenza A and RSV — multiple lines appear and both pathogens are reported as positive. This makes the 12-in-1 a true differential-diagnostic instrument rather than a single-pathogen screen.
Who is allowed to use this test?
The 12-in-1 Respiratory Multitest is CE-marked for professional use only — GP practices, paediatric clinics, hospital emergency departments, urgent-care facilities, pharmacy testing services, occupational-health providers, and long-term-care facilities. It is not intended for unsupervised self-testing at home.
How is the sample collected and processed?
Take an anterior nasal swab from both nostrils: insert the supplied sterile swab approximately 2 cm (3/4 inch) until resistance is met at the turbinates, rotate several times against the nasal wall, then repeat in the other nostril with the same swab. For young children, do not insert deeper than 1.25 cm (1/2 inch). Place the swab in the buffer tube, rotate and squeeze 5 times, leave for 1 minute, then dispense 3 drops into the test card. Read the result at exactly 10 minutes — results read after 20 minutes are invalid. Process samples within 30 minutes of collection.
How should the test be stored, and what is the shelf life?
Store the kits between 2 °C and 30 °C, protected from direct sunlight. The expiry date is printed on the outer packaging — current batch expiry: 16 April 2028. Once a foil pouch is opened, the test must be used within 1 hour. Do not freeze the kit and do not use the test if the pouch seal is damaged or the cassette is wet.
Is the test CE-certified, and in which languages is the IFU available?
Yes — the 12-in-1 Respiratory Multitest is CE-marked as an in-vitro diagnostic medical device (IVD) for professional use. The manufacturer is Shenzhen Reagent Technology Co., Ltd.; the EU authorised representative is CMC Medical Devices & Drugs S.L., Málaga, Spain. The Instructions for Use are supplied in English, German, French, Spanish, Italian, and Dutch. The included sterile swabs are EO-sterilised.
Can I order in bulk for my clinic, hospital, or pharmacy?
Yes. parahealth offers transparent volume pricing — see the discount tiers shown on this product page (lowest tier from 300 units onwards). For institutional orders, framework agreements, or pharmacy chain supply, contact our B2B team directly for dedicated quotation, guaranteed availability, and EU-wide shipping. As parahealth is the brand owner, you buy directly from us — no middlemen.
Frequently Asked Questions
Find answers to the most common questions about ordering, shipping, and our products.
Are your products clinically tested and safe?
Yes, all our medical devices and diagnostic tests undergo rigorous clinical testing and validation to ensure safety, accuracy, and efficacy. We comply with all relevant medical device regulations and quality standards.
What is your return policy?
We offer a 14-day return policy for private customers. Products must be unused and in original packaging. Please note that B2B and wholesale customers are subject to different terms. Contact our wholesale team for details.
How long does shipping take to Germany?
Standard shipping to Germany takes 1-2 business days from our Berlin facility. We also offer expedited options at checkout for faster delivery.
Do you provide support for professional/clinical use?
Yes, we offer dedicated support for healthcare professionals and clinics, including product training and technical assistance.
What are your B2B payment and shipping terms?
B2B customers receive customized payment terms and shipping arrangements. Please contact our wholesale team for details.
Do you offer bulk orders or wholesale pricing?
Yes, we offer B2B wholesale pricing for pharmacies, clinics, and medical practices. Contact us for volume pricing and terms.
Will I receive tracking information?
Yes, all orders include tracking information sent via email so you can monitor your shipment.
Do you ship internationally?
Yes, we ship worldwide from our Berlin facility. International shipping times vary by destination.
Where do you ship from?
We ship from our state-of-the-art AutoStore Warehouse in Berlin, Germany, ensuring fast and efficient order processing and delivery.
