Anesthesia Machines Suppliers & Bulk Manufacturers
Available Forms: Stationary anesthesia machines, Portable anesthesia units
Available Strengths: Advanced ventilation modes, integrated monitoring, reliable gas delivery, suitable for operating rooms and emergency settings
Reference Brands: GE Healthcare, Draeger, Mindray, Philips, Dräger
Category:
Medical Devices
Anesthesia machines deliver controlled inhalation gases, including oxygen and anesthetic agents, to induce and maintain anesthesia. They support precise ventilation, oxygenation, and monitoring, ensuring patient safety during surgery. Benefits include accurate gas delivery, consistent anesthesia depth, improved patient control, and enhanced safety for both veterinary and human healthcare providers.
Anesthesia machines is available in Stationary anesthesia machines, Portable anesthesia units
and strengths such as Advanced ventilation modes, integrated monitoring, reliable gas delivery, suitable for operating rooms and emergency 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, Anesthesia machines is supplied in
bulk quantities with complete regulatory support including DMF, COA, and MSDS.
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Technical Specifications & Supply Details
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| 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) |
Anesthesia machines 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:
Anesthesia machines in the EU and US are regulated to ensure safety, efficacy, and quality. In the US, FDA approval involves clinical validation, safety assessments, and GMP compliance. In the EU, CE marking certifies conformity with the Medical Device Regulation (MDR). These devices undergo validation, stability testing, and audits, with detailed documentation including safety profiles, performance data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to reliable, safe anesthesia systems essential for surgical safety, patient monitoring, and effective anesthesia delivery in both healthcare and veterinary practices worldwide.
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