Disposable & Safety Syringes Suppliers & Bulk Manufacturers
Available Forms: Standard disposable syringes, Safety syringes, Pre-filled syringes
Available Strengths: Typically 1 mL, 3 mL, 5 mL, and 10 mL sizes
Reference Brands: Becton Dickinson (BD), Terumo, Hospira (by Pfizer), Merit Medical
Category:
Medical Devices
Disposable and safety syringes prevent needlestick injuries by incorporating safety features like needle guards and retractable mechanisms. They reduce cross-contamination, ensure safe drug administration, and protect healthcare workers. Their use supports infection control, minimizes accidental injuries, and enhances safety during vaccinations and injections in clinical and veterinary practices.
Disposable & safety syringes is available in Standard disposable syringes, Safety syringes, Pre-filled syringes
and strengths such as Typically 1 mL, 3 mL, 5 mL, and 10 mL sizes.
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, Disposable & safety syringes 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) |
Disposable & safety syringes 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:
Disposable and safety syringes are regulated in both the US and EU, supported by dossiers demonstrating safety, efficacy, and manufacturing quality in compliance with GMP and IVDR standards. In the US, FDA approval involves clinical validation and safety assessments, while in the EU, CE marking certifies conformity with medical device regulations. These syringes undergo validation, stability testing, and quality audits, with comprehensive 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 safe, reliable syringe products essential for vaccination, drug administration, and clinical use globally, protecting healthcare workers and patients alike.
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