Physical Testing

Medical electrical equipment: Part 2 - 30 particular requirements for basic safety and essential performance of automated non - Invasive sphygmomanometers — IS/IEC 80601: Part 2: Sec 30 (2018) Testing

IS/IEC 80601: Part 2: Sec 30 (2018) is a BIS product testing standard for medical devices & textiles (1 notified product). Book laboratory testing required for ISI Mark / CRS certification.

IEC · Global

IEC (International) — typically accepted in Global. IEC methods are recognised worldwide and often underpin CE, CB Scheme and multi-market electrical / EMC filings.

Product category: Medical Devices & Textiles
Main standard: IS/IEC 80601: Part 2: Sec 30 (2018)
Test type: Physical
Accreditation: ISO/IEC 17025 / NABL (BIS-recognised labs)
Testing timeline: 7–14 working days
Sample size required: Specimen set as per standard (lab-confirmed)
Tentative testing price: ₹7L – ₹9.9L

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IS/IEC 80601: Part 2: Sec 30 (2018) laboratory testing

IS/IEC 80601: Part 2: Sec 30 (2018) is a BIS certification testing standard. Products notified under this IS must be tested in recognised laboratories before ISI Mark / CRS registration can proceed.

Discipline

Mapped under Physical Testing based on the typical product family (Medical Devices & Textiles).

What labs typically evaluate

Conformance to the clauses in IS/IEC 80601: Part 2: Sec 30 (2018)
Safety / performance / material checks required for the notified product
Report pack suitable for BIS application and surveillance

BIS products covered by this standard

Medical electrical equipment: Part 2 - 30 particular requirements for basic safety and essential performance of automated non - Invasive sphygmomanometers (ISI)

Next step

Share your product datasheet / HSN and target scheme (ISI or CRS). Certko maps the lab scope, indicative cost and booking path.

BIS products tested to this standard

1 BIS-notified product map to IS/IEC 80601: Part 2: Sec 30 (2018) — open a product for scheme, labs and indicative costs.

ISI Mark · Medical Devices & Textiles

Medical electrical equipment: Part 2 - 30 particular requirements for basic safety and essential performance of automated non - Invasive sphygmomanometers

IS/IEC 80601: Part 2: Sec 30 (2018)

FAQs about Medical electrical equipment: Part 2 - 30 particular requirements for basic safety and essential performance of automated non - Invasive sphygmomanometers — IS/IEC 80601: Part 2: Sec 30 (2018) Testing

What does “Medical electrical equipment: Part 2 - 30 particular requirements for basic safety and essential performance of automated non - Invasive sphygmomanometers — IS/IEC 80601: Part 2: Sec 30 (2018) Testing” cover?

Medical electrical equipment: Part 2 - 30 particular requirements for basic safety and essential performance of automated non - Invasive sphygmomanometers — IS/IEC 80601: Part 2: Sec 30 (2018) Testing covers the key parameters for this product/test type under IS/IEC 80601: Part 2: Sec 30 (2018). Review the writeup on this page for scope details, then request a quote for your exact sample.

Which accreditation applies?

This scope is typically run in ISO/IEC 17025 / NABL (BIS-recognised labs) accredited laboratories. Confirm the exact lab and NABL scope on your quotation.

How do I get a quote for this test?

Use Get Expert Help / Contact with your product name, target market and any buyer specification. We map the lab, sample size and indicative turnaround.

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