Conditions for using this special access route (SAR)
In an emergency or when all available medical therapies fail, a doctor or dentist may request for dealers to import unregistered medical devices for his patient. Approval from HSA is needed for such scenarios.
The qualified practitioner needs to provide clinical justification that the unregistered medical devices are required to meet special clinical needs arising in the course of his practice, which includes the following:
This includes:
- Absence of alternative treatment option; or
- Available alternative treatments failed or deemed ineffective or unsuitable for the patient according to the doctor’s or the dentist’s clinical judgement; and
- Patient’s health will be clinically compromised without the requested treatment
The unregistered medical device is needed to minimise disruption to the continued supply of a similar registered medical device
- Absence of registered alternatives or lack of a specific feature in registered medical device; or
- Available registered medical devices or models are deemed
ineffective or unsuitable for the patient according to the doctor’s or
the dentist’s clinical judgement; or
- User’s (doctor or dentist) familiarity or expertise in terms of
device technology, design and/or operation that is likely to support or
enhance the safety outcomes of the procedure or treatment for the
patient; and
- Patient’s health will be clinically compromised without the requested medical device
The unregistered medical device was used:
- Before 1 January 2012
- In a licensed private hospital as approved by the relevant authority of that healthcare institution
- In a licensed medical clinic as required by the doctor or dentist
- And there are no known safety issues.
The dealer and the qualified practitioner needs to ensure that the unregistered medical device complies with other regulatory requirements such as the Radiation Protection Act governed by the National Environment Agency.
Capital equipment (e.g. X-ray machines, CT scanners, MRI machines) would not qualify for this SAR. Product registration is required for such devices.
Note: The safety and performance of the device is not assessed by us during application review.
Import, supply and manufacture of drug of abuse test kits needs additional controlled drug licences under the Misuse of Drugs Act besides licences under Health Products (Medical Devices) Regulations. For more information on controlled drug licence application, please contact the Licensing and Certification Branch at Email: hsa_certification@hsa.gov.sg.
You should register your medical device if you intend to supply it on a long-term basis.
Eligibility
You must have a certified quality management system e.g. to the requirements of Good Distribution Practice for Medical Devices (GDPMDS).