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BiPAP Advance BA08.
A clinically validated bipap machine from ResMed. Built for reliability across home, clinic, and hospital settings — the same device that runs in European private hospitals is the one GHM ships to a tender in Algiers, Cairo, or Riyadh.
- IPAP
- 4-25 cmH2O
- EPAP
- 4-20 cmH2O
- Modes
- S / S-T / T / CPAP
Medical-grade, uncompromised.
CE · ISO 13485 · EU MDR
Every BiPAP Advance BA08 shipped by GHM is verified against the latest European regulatory frameworks. The documentation trail is ready on day one.
Source-to-site traceable
Audited supplier since 2024. Factory QC → Hong Kong distribution → your hospital stockroom. Every handoff logged.
Bank-verifiable invoicing
Commercial invoice includes HS code 9019.20, Incoterms 2020, country-of-origin, and HSBC trade reference.
What ships, what's certified, what's priced.
Every line below is what we attach to the commercial invoice and the technical compliance matrix. Tender-grade revisions are released by our compliance desk under NDA.
- Product name
- BiPAP Advance BA08
- Manufacturer model
- GHM-BIPAP-BA08
- Manufacturer
- ResMed
- Therapy category
- Respiratory Care
- Sub-category
- bipap machine
- IPAP
- 4-25 cmH2O
- EPAP
- 4-20 cmH2O
- Modes
- S / S-T / T / CPAP
- Build certification
- ISO 13485 quality system
- Electrical safety
- IEC 60601-1 (medical electrical equipment)
- CE marking
- EU MDR 2017/745
- Notified Body
- TÜV SÜD · TÜV Rheinland · BSI · IMQ · DEKRA — exact NB number on the Declaration of Conformity
- Quality management system
- ISO 13485 — manufacturer-certified
- UDI carrier
- Per individual carton, scannable
- Declaration of Conformity
- Released with shipment under NDA
- HS code
- 9019.20
- Incoterms
- 2020 — destination-specific (EXW / FOB / CIF / DAP)
- Country of origin
- Per manufacturer Declaration
- Bank reference
- HSBC Hong Kong on commercial invoice
- Shipping packaging
- Manufacturer original — bonded warehouse staged
- Lead time
- Quoted per RFQ — typically 4–8 weeks ex-Hong Kong
- Minimum order quantity
- Tender-tier or single-practice — quoted per RFQ
Everything a compliance desk needs.
Tender-grade documentation is released by our compliance desk under NDA, with the latest revision and the manufacturer's Notified Body reference attached. One reply, one bundle.
Documentation is the manufacturer's — not GHM's. We forward the file revision active at the date of your enquiry, with the NB number and validity dates clearly visible on the first page.
