Technology / product information

Medical suction systems require strict cleanliness and stable assembly to ensure safety in operating rooms and emergency care.
SIMA Technology, located in Nakhon Ratchasima, Thailand, provides medical device assembly for Disposable Liner + Canister sets, essential components used in liquid-collection systems for hospitals and critical-care facilities.

⚠️ Challenges in Medical Device Assembly
Many companies import finished products, which results in:
- Limited quality control
- Risks of leakage or loose assembly
- Long international lead times
- Difficulty handling design updates

Moving the assembly to a certified cleanroom in Thailand helps improve quality, reduce risk, and shorten delivery time.

🔧 Components of a Suction System
A complete set includes:
- Disposable Liner (single-use soft bag from supplier)
- Canister (hard-plastic container assembled in-house)
- Valve / Connector / Filter

Each interface must be assembled accurately, as even a minor leak can compromise safety in medical environments.

🔵 Cleanroom Assembly Process
SIMA performs assembly in a dedicated medical cleanroom with the following process control:
1. Incoming inspection (visual + dimensional)
2. Liner-to-Canister assembly
3. Installation of valves, filters, connectors
4. Leakage-related and functional testing according to customer requirements
5. Packaging with barcode traceability

This process supports both small-batch runs and full mass-production.

📑 Evidence / Certification
- Cleanroom designed for medical device assembly
- Leakage-related testing per customer specifications
- Documentation and traceability under ISO 13485:2016
- Supports OEM export customers
[1][2]

📌 Suitable Applications
Ideal for medical manufacturers needing cleanroom outsourcing:
- Operating-room suction systems
- Suction units for respiratory use
- Disposable liner systems for ICU / ER
- Semi-assembly or full assembly based on OEM specifications

⚙️ Comparison — Importing FG vs Assembly in Thailand
❌ Importing Finished Goods
- High cost
- Limited QC
- Long lead time
- Difficult to implement design changes

✅ SIMA Assembly in Thailand
- Better cost control
- Cleanroom + ISO 13485 compliance
- Faster delivery
- Supports engineering change and test runs

🤝 Trust
“According to Mr. Waranon – Expert Engineer at SIMA Technology, the assembly of Disposable Liner + Canister is carried out in a cleanroom operating under ISO 13485, with component inspection, controlled assembly steps, and functional testing based on customer specifications to ensure medical-grade reliability.”
[1][2]

📞 Contact & More Information
For technical details or project consultation, please contact our sales team or download additional information below.

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❓ FAQ

Q1: Does SIMA manufacture the Disposable Liner bag?
No. Liner bags are sourced from approved suppliers and assembled with the Canister in the cleanroom.

Q2: Does SIMA perform leakage testing?
Yes. Leakage-related tests are performed according to customer requirements.

Q3: Do you support Full Assembly?
Yes. Both Partial Assembly and Full Assembly are supported based on the customer’s specification.

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🔗 Related Knowledge (Cluster Internal Link)
• Knowledge Basic:
• Knowledge Advance:

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📚 Glossary
- Disposable Liner: Single-use flexible bag component
- Canister: Rigid container used with the liner
- Cleanroom Assembly: Controlled-environment assembly process
- ISO 13485: Medical Device Quality Management System
- Functional Test: Operation-based performance verification
- Traceability: Production tracking via coded identifiers

Reference
[1] Process Capability & Test Report – Medical Assembly Line (2025) — Internal Validation
[2] ISO/EN 13485:2016 — International Organization for Standardization

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Updated: 2025-11-13