Pacific Hospital Supply Co., Ltd.
Pahsco 是医院一次性医疗用品、医疗设备和集中医用气体管道系统的主要供应商
Pahsco 是医院一次性医疗用品、医疗设备和集中医用气体管道系统的主要供应商。凭借 GMP、ISO 13485 和 MDR 认证，我们展示了我们对质量坚定不移的承诺。我们的综合服务涵盖开发、设计、生产和销售。作为行业领导者，我们是全球医疗保健客户值得信赖的合作伙伴，向 80 多个国家和地区出口多样化产品。选择 Pahsco 以获得可靠的医疗解决方案。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Taipei, Taiwan
- Website
- https://pahsco.com.tw
- Categories
- 消费电子产品
- Markets
- 台湾
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- export-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- registry-active-global (green), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- registry-change-published (green), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- officer-appointed (green), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- ownership-on-record (green), checked 2026-08-20 Taiwan Ministry of Economic Affairs, Commerce Development Administration (經濟部商業發展署), company registration open data (GCIS)
- facility-registered (green), checked 2026-09-19 Taiwan Industrial Development Administration, registered factory directory (status: producing)
- registry-id-verified (green), checked 2026-09-19 Taiwan International Trade Administration, import/export firm registry (BOFT)
- registry-activity (green), checked 2026-09-19 Taiwan Ministry of Finance, national business tax registration
Import rules for these goods
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)