China Stainless Steel
Stainless Steel
Medical Devices
& Components
TeCarve provides a comprehensive range of medical devices and components, widely applied in surgical operations, interventional therapy, and diagnostic procedures.
Our products include:
Disposable Syringes & Needles (HS 90183100 / 90183210 / 90183220)
Catheters & Tubes (HS 90183900)
Endoscopes & Spare Parts (HS 90189030)
Other Medical & Surgical Instruments (HS 90189099)
Radiopaque Markers made of Stainless Steel, Platinum-Iridium, Tantalum, Niobium (HS 81039990, 81129940, 71101990)
Titanium & Nickel Alloys for surgical applications (HS 810890, 7505, 75071200)
Stainless Steel Flexible Hoses for medical fluid systems (HS 83071000)
We offer both finished medical devices and critical OEM components, supporting global medical manufacturers and distributors.
Order Information
| Standards | Reference standards vary by project and must be confirmed per order |
|---|---|
| Origin | China |
| Lead Time | 10-25 days after deposit for most orders |
| MOQ | Typically 100-300 kg depending on product type |
Classification
Category A: Medical Devices (Finished Products)
Syringes, Needles, Catheters, Endoscopes
Category B: Medical Components (OEM Parts)
Radiopaque Markers (Stainless Steel, Platinum-Iridium, Tantalum, Niobium)
Titanium / Nickel alloy tubes, rods, wires for surgical use
Category C: Accessories & Assemblies
Stainless steel flexible hoses for medical fluid handling
Depending on the component design, material, intended use, and customer requirements, relevant project references may include:
- ISO 10993 series: Reference framework for biological evaluation of finished medical devices; applicability and testing are project-specific.
- ASTM F67 / F136: Reference specifications for specified titanium materials used in surgical implant applications; material conformity must be confirmed for each order.
- ASTM F75: Reference specification for cobalt-chromium alloy; material conformity must be confirmed for each order.
- EN ISO 9626: Reference standard for stainless steel needle tubing; applicable requirements must be confirmed for each project.
Reference Standards
Project Documentation
Documentation requirements vary by component, material, intended use, and destination market. Please provide the applicable specifications with your drawing or sample so available material and inspection documentation can be confirmed before quotation.
| Standard | Scope |
|---|---|
| ISO 10993 series | Biological evaluation of medical devices; applicability and testing are project-specific |
| ASTM F67 | Unalloyed titanium for surgical implant applications |
| ASTM F136 | Wrought Ti-6Al-4V ELI alloy for surgical implant applications |
| ASTM F75 | Cobalt-chromium-molybdenum alloy castings for surgical implants |
| EN ISO 9626 | Stainless steel needle tubing for the manufacture of medical devices |
| ASTM F899 | Wrought stainless steels for surgical instruments |
Material conformity to the applicable standard must be confirmed for each order; reference standards vary by component design, material, and intended use.
General Surgery (syringes, needles, suturing)
Interventional Cardiology (catheters, guidewires, radiopaque markers)
Endoscopy (diagnostic & therapeutic scopes)
Orthopedic & Dental Implants (titanium & nickel alloys)
Medical Fluid Systems (stainless steel flexible hoses)
Applications
For precision medical device manufacturing, review how OEM buyers can verify our cleanroom handling, micro-machining tolerances, passivation testing, and material traceability.
Key Advantages
Full supply chain coverage: from raw material to finished device
High-precision machining (tolerance down to ±0.01 mm)
Material and documentation requirements are confirmed for each application and order
Competitive cost advantage from China-based manufacturing
Export experience covering Europe, U.S., Middle East, and Asia
HS Codes covered: 90183100, 90183210, 90183220, 90183900, 90189030, 90189099, 83071000, 7505, 75071200, 810890, 81039990, 81129940, 71101990
Export Markets: EU, USA, Turkey, India, Middle East
Trade Terms: FOB / CIF / DDP available
Packaging: Sterile pack for medical devices, industrial pack for metallic components
Export Information
packaging
PVC Wrapping
& End Caps
Custom Barcoding
& Labeling
Anti-Corrosion
& Moisture Protection
Seaworthy Wooden Cases & Pallets
Medical Components Inspection & Traceability Photos
Real factory, inspection, packaging and loading photos from TeCarve gallery pages.



Tailored Solutions, Timely Fulfillment
CUSTOMIZATION
& DELIVERY
Customization Process
TeCarve supports custom medical-device components based on customer drawings or approved samples. The process begins with a review of geometry, material, surface finish, tolerances, intended application, and required documentation. After technical requirements are confirmed, the project can proceed through sample or prototype review, production, inspection, and delivery preparation. Relevant material standards, such as ASTM F899 for wrought stainless steels used in surgical instruments, can be reviewed as project references where applicable; conformity must be confirmed for the selected material and order. Contact us to discuss the requirements for your component.
Low MOQ & Rapid Prototyping
Small batch customization and sample production are supported, helping you shorten your development cycle and market entry.
Optimized Lead Time
Most medical device components and finished products ship within 10–25 days after deposit, consistent with TeCarve's standard lead time across product lines. Exact timing depends on component complexity, required documentation, and order volume.
Global Logistics & On-Time Delivery
For medical device component deliveries to international markets, anti-corrosion and moisture protection is paired with custom barcoding and labeling for clear material and component identification.
Frequently Asked Questions
What is the difference between TeCarve's medical device categories?
TeCarve organizes medical components into three categories: Category A covers finished medical devices such as syringes, needles, catheters, and endoscopes; Category B covers OEM components such as radiopaque markers and titanium/nickel alloy tubes, rods, and wires for surgical use; Category C covers accessories and assemblies such as stainless steel flexible hoses for medical fluid handling.
What materials does TeCarve supply for medical device components?
TeCarve supplies stainless steel, titanium, and nickel alloys for surgical applications, along with radiopaque markers in stainless steel, platinum-iridium, tantalum, and niobium, depending on the component's intended use and required imaging visibility.
What standards apply to TeCarve's medical device components?
Depending on the component, material, and intended use, relevant project references may include the ISO 10993 series for biological evaluation, ASTM F67 and ASTM F136 for titanium implant materials, ASTM F75 for cobalt-chromium alloy castings, EN ISO 9626 for stainless steel needle tubing, and ASTM F899 for wrought stainless steels used in surgical instruments. Applicability and material conformity must be confirmed for each order.
What is the MOQ and lead time for medical device components?
MOQ is typically 100–300 kg depending on product type, with low-MOQ and rapid prototyping support available for small batch customization and sample production. Most orders ship within 10–25 days after deposit.
Does TeCarve provide documentation for material traceability?
Yes. Documentation requirements vary by component, material, intended use, and destination market. TeCarve confirms available material and inspection documentation, including traceability records, against the applicable specification before quotation.

