Assembly line inside the anti-static workshops

One-Stop-OEM/ODM für Hausmedizingeräte

Von der Produktdefinition bis zum zugelassenen Produkt in Ihrer Verpackung: Design, Formenbau, Zulassung, klinische Nachweise, Fertigung und Logistik.

Four services, one programme

Research and regulatory: product preliminary research, CRO services, clinical trials, testing and certification.
Design and engineering: appearance, structural, brand and packaging design; electronics, embedded and mobile software development; prototype and performance testing.
Manufacturing: mould design and development, in-house injection moulding, assembly, packaging and inspection.
Logistics and finance: medical-device-compliant warehousing, import/export customs handling, and supply-chain finance to improve your working capital turnover.

How a programme runs

1. Requirement review — target market, channel, price band and regulatory route.
2. Product definition — select a platform from the catalogue or scope a new one.
3. Industrialisation — tooling, packaging artwork, firmware and app configuration.
4. Verification — performance, safety and EMC testing with documented results.
5. Regulatory submission — FDA, EU MDR, NMPA or your national registration, supported by our technical file.
6. Production and delivery — ramp from pilot lots to volume, with export documentation.

Commercial terms

Item	Detail
Lead time	3-15 days for core components, supported by strategic chip stock
Order volume	Hundreds to hundreds of thousands of units
Customisation	Cuff, housing, display, language pack, app skin, packaging and instruction manual
Regulatory support	FDA, EU MDR CE, NMPA, plus CFS and FCC documentation
Tooling	Own mould shop — tooling cost and ownership agreed per project

Intellectual property

We hold 23 patented technologies in infrared sensor temperature measurement and photoelectric physiological monitoring. Tooling and product IP ownership is agreed in writing at project start — we do not sell a customer-specific design to another customer.

What is the minimum order quantity?

MOQ depends on whether you take a catalogue platform or a fully custom tooling project. Catalogue platforms start substantially lower than new-tooling projects. Send us the model and target market and we will confirm the exact MOQ.

Can you support registration in our country?

Yes. We provide the technical file, test reports and declarations that a distributor or notified body requires, and we have done this for FDA, EU MDR and NMPA submissions.

Do you do private label?

Yes — housing silkscreen, display language pack, app skin, packaging and instruction manual can all carry your brand.

How do we start?

Send your target market, product interest and expected volume. We will come back with the closest catalogue platform, indicative MOQ and lead time.

Fertigungsnetzwerk

„2+1“-Produktionsnetzwerk über drei Regionen

Vier Standorte, ein Qualitätsstandard — GMP-zertifizierte Produktion in Shenzhen, lokalisierte Schlüsselkomponenten in Vietnam und ein neuer Standort in Zhongshan im Bau.

**Shenzhen-Zentrale**160.000 m² große GMP-zertifizierte Fertigung

**Shenzhen II (AOJ Health)**Serienfertigung, 2 Mio. Einheiten/Jahr

**Vietnam AOJ**Lokalisierte Schlüsselkomponenten-Fertigung für reibungslose COO-Zertifizierung

**Zhongshan AOJ (im Bau)**100.000 m² GMP-Werk, 8 Mio. Einheiten/Jahr geplant

Digitalisierte Produktionslinie

Jede Linie läuft mit digitalem Kanban-Board

Jede Montagelinie wird von einem digitalen Kanban-Board gesteuert: Auftragsfortschritt, Stundenleistung, Taktzeit und Inline-Qualitätsdaten werden in Echtzeit an der Linie angezeigt. Materialien werden Station für Station nachgerufen, Abweichungen lösen sofort Andon-Meldungen aus, und dieselben Daten fließen in die Chargenrückverfolgung — Marken können Liniendaten jederzeit prüfen, nicht nur fertige Einheiten.