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Jiangsu Zhiyu Medical Instrument Co., Ltd. is a Medical Consumables manufacturer based in Taixing, Jiangsu, China. We produce single-use sterile consumables for injection, infusion, irrigation, oral dosing and clinical protection, supplying hospitals, clinics, distributors, government procurement programs and OEM/ODM brand owners worldwide.
Our Medical Consumables Range
Our Medical Consumables category covers the core single-use products required for daily clinical operations. The range is organized into six supplied sub-categories, each addressing a defined clinical or channel requirement. We maintain flexible specifications so that standard configurations and project-specific variants can be sourced through one manufacturing entry point.
| Sub-category | Typical Products | Primary Application Fit |
|---|---|---|
| Disposable Syringes | Standard sterile, auto-disable, safety, oral/feeding, irrigation syringes | General injection, immunization programs, oral medication, flushing and nursing support |
| Insulin Syringes | 0.3 mL, 0.5 mL, 1 mL fixed-needle syringes with U-100 graduations | Subcutaneous insulin delivery, pharmacy channels, chronic disease management |
| OEM/ODM Needle-Free Injectors Factory in China | Needle-free injector units, disposable plastic ampoules, vial adapter transfer devices | Needle-free drug delivery systems, differentiated injection product lines, system-based procurement |
| Medical Needles & IV Products | Hypodermic needles, butterfly needles, safety needles | Venipuncture, intravenous access, injection procedures, needle safety programs |
| Infusion Sets | Gravity infusion sets and related accessories | Intravenous fluid administration, ward and outpatient infusion therapy |
| Medical Protective Products | Selected single-use protective items | Infection control, clinical protection, general medical supply programs |
Application Fit Across Clinical Settings
Each sub-category is designed around a specific clinical workflow. Standard sterile syringes handle routine aspiration, injection and medication preparation. Auto-disable syringes support immunization and public health programs where reuse prevention is required. Safety syringes add needlestick protection for occupational exposure reduction. Oral and feeding syringes serve liquid medication management, elderly care and pediatric dosing. Irrigation syringes cover flushing and nursing assistance.
Insulin syringes address the precision requirements of subcutaneous insulin therapy, with small-volume barrels, U-100 unit graduations and short, fine fixed needles. Needle-free injectors provide a system-based alternative for drug delivery without traditional metal needles, combining a main unit with disposable ampoules and transfer devices. Hypodermic and butterfly needles support venipuncture and intravenous access, while infusion sets complete the intravenous therapy chain. Protective products support infection control alongside the consumable range.
Critical Specifications and Configuration Options
We configure each product around the working point, material and production target. The specification variables below are confirmed during project evaluation so that the delivered product matches the clinical and regulatory requirements of the target market.
- Volume range: standard syringes commonly cover 5 mL, 10 mL, 20 mL and 30 mL; oral and feeding syringes cover 1 mL to 50 mL; insulin syringes cover 0.3 mL, 0.5 mL and 1 mL.
- Needle configuration: with needle or without needle, fixed needle, Luer Slip or Luer Lock interface, and compatibility with standard or safety needles.
- Needle gauge and length: insulin needles typically range from 27G to 31G with short lengths such as 8 mm and 12.7 mm; hypodermic and butterfly needles are specified by gauge and length according to the procedure.
- Safety features: standard, auto-disable and safety mechanisms are available across the syringe range.
- Graduation and scale: clear unit markings for insulin products and readable volume graduations for general syringes.
- Packaging: neutral packaging, color box, blister or PE bag options, with multilingual label design and private-label support.
Manufacturing, Quality Control and Compliance
Zhiyu operates a collaborative production system covering injection molding, assembly, testing and packaging on related product lines. Automated equipment, online testing and standardized quality control processes support consistency in batch manufacturing. Our in-house laboratory and testing center follows a structured workflow covering incoming material inspection, in-process inspection and final product inspection. Samples and finished products are retained according to internal procedures, and inspection records, quality reports and testing documentation are archived.
For applicable product lines, we hold ISO 13485:2016 certification, EU MDR certification under Regulation (EU) 2017/745, FDA 510(k) clearance for specified sterile syringe and hypodermic needle products, and FDA establishment registration and device listing. Regulatory scope differs by product line and target market, so applicable documents are confirmed against the specific product and destination during project evaluation.
OEM/ODM and Custom Development Support
Beyond standard supply, we support OEM and ODM cooperation across different product lines. Our project-based capabilities cover packaging adaptation, specification expansion, private-label support, mold development for applicable projects, structural optimization and customized product development. We help customers move from product concept to sampling, validation and large-scale production.
Custom development is evaluated against the application scenario, target market and business conditions. For injection-molded components, needle-related products and related consumables, we can assess structural changes, proprietary specifications and customized packaging requirements. This support is suited to distributors and brand owners building differentiated product lines or entering specific market segments.
Information We Use to Configure Your Solution
To prepare an accurate configuration and quotation, we evaluate the following project inputs. Early clarification of these points allows us to confirm specifications, packaging and production planning more efficiently.
| Project Input | What We Confirm |
|---|---|
| Product name and sub-category | Range selection and applicable product line |
| Size, volume or dimensions | Barrel capacity, graduation system and unit markings |
| Needle type, gauge and length | Needle configuration, interface type and compatibility |
| Packaging requirements | Packaging format, labeling and private-label options |
| Target market | Applicable regulatory documents and compliance scope |
| Estimated order quantity | Production planning and batch scheduling |
| OEM/private label requirement | Customization scope and development path |
| Drawings, photos or reference samples | Structural evaluation and sampling direction |
Documentation, Packaging and Delivery Scope
We support registration, tender and distributor review with quality-related documents for applicable product lines. Packaging adaptation covers neutral packaging, color box, blister and PE bag formats, with multilingual label design and OEM/ODM packaging support. Delivery scope is confirmed per project based on product type, order quantity, specification complexity and packaging requirements.
Frequently Asked Questions
What products does Zhiyu supply in the Medical Consumables range?
We supply disposable syringes, insulin syringes, needle-free injectors and their consumables, hypodermic and butterfly needles, infusion sets and selected protective products. The range covers injection, infusion, irrigation, oral dosing and infection control applications for hospitals, clinics, distributors and procurement programs.
Do you support OEM and ODM projects?
Yes. We support OEM and ODM cooperation covering packaging adaptation, specification expansion, private-label support, mold development for applicable projects, structural optimization and customized product development. Projects progress from concept and sampling through validation to mass production.
Which quality and regulatory documents apply to your products?
For applicable product lines we hold ISO 13485:2016, EU MDR, FDA 510(k) clearance for specified sterile syringe and hypodermic needle products, and FDA establishment registration and device listing. Regulatory scope differs by product and target market, so applicable documents are confirmed per project.
How do you control product quality during batch manufacturing?
We operate an in-house laboratory and testing center with incoming material inspection, in-process inspection and final product inspection. Automated equipment, online monitoring and automatic vision inspection are used at key production stages for applicable products. Samples and finished products are retained according to internal procedures, with inspection records and quality reports archived.
Can you provide samples before a production order?
Sample arrangements depend on the product. For standard products, samples can usually be prepared from existing specifications. For customized projects, we confirm the application scenario, specification requirements, packaging method and target market first so that suitable samples or trial solutions can be prepared.
What information should be included in a quotation request?
Provide the product name, size or dimensions, needle type and gauge, with or without needle, packaging requirements, target market, estimated order quantity and whether OEM or private label is needed. Drawings, photos or reference samples help us evaluate customized projects more accurately.
