Test Price
1,800 AED✅ Home Collection Available
C7 Complement Test in UAE | 1800 AED | DHA Licensed Diagnostic Service
Executive Summary & Core Metrics
Executive Summary: The C7 Complement Test achieves 99.9% diagnostic sensitivity through ISO-accredited processing. Services include VIP Mobile Phlebotomy with temperature-controlled cold-chain home collection (available daily 8 AM–11 PM), telephonic post-test clinical guidance, and direct insurance billing verification via WhatsApp +971 54 548 8731.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital‑Grade Home Collection via ISO Certified Cold‑Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post‑Test Clinical Guidance for result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The C7 Complement Test measures the serum level of complement component C7, a critical protein in the terminal complement pathway. Deficiency predisposes individuals to severe, recurrent Neisseria meningitidis infections and is essential for timely immunodeficiency work‑up. The assay uses Radial Immunodiffusion (RID) with nephelometric confirmation, offering 99.9% sensitivity for isolated C7 deficiency.
| Feature | Our C7 Complement Test | Standard Total Complement Panel |
|---|---|---|
| Methodology | Radial Immunodiffusion (RID) with Nephelometry Confirmation | Broad‑range haemolytic or CH50 assay (not specific for C7) |
| Diagnostic Precision | 99.9% sensitivity for isolated C7 deficiency | May miss low‑level component deficiencies |
| Turnaround Time | 14–21 business days after sample reception (send‑out reference lab) | 3–5 days locally |
| Sample Volume | 2 mL serum (0.5 mL minimum) – cold‑chain transport required | Usually 1–2 mL serum |
| Regulatory Compliance | DHA‑compliant, ISO 9001:2015, UAE PDPL & Federal Health ICT Law | Basic privacy adherence |
Physician Insight & Safety Protocols
“C7 complement testing is a vital investigation for patients with unexplained recurrent meningococcal disease. A low result must be evaluated alongside a detailed infectious history and genetic counselling. Early detection enables prophylactic measures and timely immunization, potentially saving lives.”
— Dr. Ajay Singh, General Practitioner, DHA Reg. No. 36234132
⚠️ Medication Advisory
Do not discontinue prescribed medication without consulting your physician.
Complement testing requires clinical correlation before any therapeutic change. Immunomodulatory drugs may suppress C7 synthesis; a doctor’s note is required for accurate test interpretation.
Safety Precautions & Exclusion Criteria
- Exclusion Criteria: Active febrile illness or recent vaccination (within 4 weeks) may transiently alter complement levels. Postpone unless medically urgent and cleared by your physician.
- Emergency Red Flags: If you develop sudden high fever, severe headache, neck stiffness, confusion, or a purplish rash after sample collection, go immediately to the nearest emergency department.
- Mandatory Consent: A duly filled Test Send Out Consent Form (Form 35) is compulsory before collection.
Patient FAQ & Clinical Guidance
1. What does a low C7 complement level mean?
A low C7 complement level indicates a probable deficiency, putting you at heightened risk for life‑threatening Neisseria infections such as meningitis. Follow‑up with a specialist and genetic counselling is recommended.
2. Why does this test require a special consent form and cold shipping?
Because C7 is heat‑labile and the test is sent to a reference lab, Form 35 ensures legal and traceable chain‑of‑custody, while refrigerated transport preserves specimen integrity for accurate results.
3. How should I prepare for the C7 blood draw?
No fasting is required, but you must inform the phlebotomist about any recent infections or medications. The signed Consent Form 35 must be ready before the home visit (8 AM–11 PM daily).
UAE Regulatory & Data Privacy Adherence
All testing and data handling comply with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. Our laboratory operates under ISO 9001:2015 certification (INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | C7 Complement (Serum) |
| Price (AED) | 1,800 AED |
| Turnaround Time | 14–21 business days (reference lab send‑out) |
| Sample Type / Matrix | Serum (2 mL; 0.5 mL minimum) |
| Methodology Used | Radial Immunodiffusion (RID) with Nephelometry Confirmation |
| ICD-10-CM Code | D84.1 (Defects in the complement system) |
| LOINC Code | 30155-4 (Complement C7 [Mass/volume] in Serum) |
| DHA Facility License & Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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