Suction Machines Suppliers & Bulk Manufacturers
Available Forms: Portable suction units, Wall-mounted suction devices, Surgical suction aspirators
Available Strengths: Variable vacuum levels (−80 to −120 mmHg), portable or stationary
Reference Brands: Stryker, Welch Allyn, Laerdal, PulmoAide (by Philips), Invacare
Category:
Medical Devices
Suction machines work by creating negative pressure to remove mucus, fluids, or gastric contents from the airway, wound, or surgical site. They help maintain clear airways, support breathing, prevent aspiration, and aid wound healing. Benefits include rapid fluid removal, improved patient safety, and enhanced clinical outcomes in medical and veterinary care.
Suction machines is available in Portable suction units, Wall-mounted suction devices, Surgical suction aspirators
and strengths such as Variable vacuum levels (−80 to −120 mmHg), portable or stationary.
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, Suction machines is supplied in
bulk quantities with complete regulatory support including DMF, COA, and MSDS.
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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) |
Suction 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:
Suction machines in the EU and US are regulated to ensure safety, efficacy, and manufacturing quality. In the US, FDA approval involves clinical validation, safety assessments, and GMP compliance. In the EU, CE marking certifies conformity with in vitro diagnostic, medical device, and safety regulations. Devices undergo validation, stability testing, and audits, with comprehensive 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 suction devices for medical and veterinary applications worldwide, supporting infection control, emergency intervention, and clinical care.
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