AiMeD Welcomes DGHS Ban on Reuse of Single-Use Medical Devices

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AiMeD has welcomed a Directorate General of Health Services directive prohibiting the reuse of single-use medical devices and disposable surgical items across public and private healthcare organisations. Rajiv Nath, Forum Coordinator of AiMeD, said reuse carries infection and device-failure risks and that liability should rest with whoever reuses a device against its labelling. The industry body has also asked for regular inspections, traceable records, action under the Medical Devices Rules, 2017 and the Clinical Establishments Act, 2010, and support for affordable single-use alternatives.

Oct 23, 2026 · 2 min read

AiMeD welcomes DGHS directive prohibiting reuse of single-use medical devices

New Delhi, October 23

The Association of Indian Medical Device Industry warmly welcomes the Directorate General of Health Services' directive of October 16, 2026, to all States and UTs, the DCGI and CGHS, prohibiting reuse of single-use medical devices and disposable surgical items in all healthcare organisations, public and private.

Reusing a device designed and validated for one use is a patient safety risk. Such devices are not built to be cleaned, resterilised or reused, and reuse can cause cross-infection, device failure, loss of performance and harm to patients. AiMeD thanks the Government for the directive, which asks that these devices be used strictly according to the manufacturer's instructions.

Rajiv Nath, Forum Coordinator, AiMeD, said: "This is a patient-first decision. Single-use means single-use. Where a product is used contrary to its labelled instructions, such as being reused, any failure or harm cannot be attributed to the manufacturer. Responsibility must rest with the person or establishment that reused it. We ask that this be clearly reflected in enforcement and in any liability framework."

AiMeD recommended strict, regular inspections of healthcare establishments, with traceable records of device use and disposal; Clear action under the Medical Devices Rules, 2017 and the Clinical Establishments Act, 2010 against reuse; Awareness and training of hospital staff on infection prevention and biomedical waste handling; A clear statement that manufacturers are not liable for failures arising from reuse contrary to labelling; and support for safer and more affordable single-use alternatives, so that cost is no reason to reuse.

— ANI

Reader’s Guide · AI-assisted, based only on the report above

What the report makes clear: A central health directive now bars reuse of single-use medical devices in public and private hospitals, and an industry body has endorsed it.

Still open: The report does not yet say how the directive will be enforced, what penalties apply, or when compliance checks begin.

Another way to look at it: Stricter single-use rules raise costs for smaller clinics, so affordable alternatives and training may decide how well the directive works.

How can hospitals balance patient safety with the cost of single-use devices?

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AiMeD Welcomes DGHS Ban on Reuse of Single-Use Medical Devices

AiMeD welcomes DGHS directive prohibiting reuse of single-use medical devices

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