Incubators (Lab & Neonatal) Suppliers & Bulk Manufacturers
Available Forms: Laboratory incubators, Neonatal incubators
Available Strengths: Accurate temperature control, humidity management, oxygen regulation, neonatal-specific features, FDA approval, and reliability for clinical and research settings
Reference Brands: Newborn, Dräger, Bariatric, AmSafe, VWR
Category:
Medical Devices
Incubators provide a controlled environment by regulating temperature, humidity, and airflow, essential for microbial, cell culture, and neonatal care. They support optimal growth, prevent contamination, and ensure safety. Benefits include reliable conditions, improved research accuracy, and enhanced health outcomes for premature and fragile neonates.
Incubators (Lab & Neonatal) is available in Laboratory incubators, Neonatal incubators
and strengths such as Accurate temperature control, humidity management, oxygen regulation, neonatal-specific features, FDA approval, and reliability for clinical and research settings.
Sourced from GMP-certified and ISO-compliant manufacturers, this API meets
global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical
formulation and commercial manufacturing, Incubators (Lab & Neonatal) is supplied in
bulk quantities with complete regulatory support including DMF, COA, and MSDS.
|
Technical Specifications & Supply Details
|
| Lead Time |
7 to 60 days (depending on batch size & schedule) |
| MOQ |
As per manufacturer’s batch size |
| COA |
Available with every batch |
| Regulatory Dossier / DMF |
Available upon request |
| Export Documentation |
FSC, COA, Manufacturing License, Product Permission |
| Standards |
IP, BP, USP |
| Certifications |
WHO-GMP, EU-GMP, USFDA (as applicable) |
Incubators (Lab & Neonatal) can be exported to over 30 countries across Asia, Africa, Europe,
and Latin America. Flexible packaging, competitive pricing, and a verified supplier
network make Pharmatradz a trusted sourcing partner for pharmaceutical companies
and contract manufacturers worldwide.
Product Description:
Lab and neonatal incubators in the EU and US are regulated to ensure safety, accuracy, and manufacturing quality. In the US, FDA approval involves validation, safety testing, and GMP compliance, especially for neonatal versions. In the EU, CE marking certifies conformity with in vitro diagnostic and medical device standards under MDR. These incubators undergo validation, stability testing, and audits, with detailed documentation including safety profiles, performance data, and manufacturing practices. For licensing procedures, approved dossiers, and regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to reliable, safe incubators vital for research, neonatal care, and laboratory diagnostics worldwide, supporting optimal microbial, cell culture, and patient outcomes.
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