Holter Recorder [Electrocardio-gram Recorder]
- UID
- IMP/MD/2023/001133_b5f89bb2e669fffab1561d46c0fc19dd_94a4fa8abe35f02ba61e922ce4b117b3
- Device class
- Class B
- Brand name
- ePatch
- License holder
- PHILIPS INDIA LIMITED
- Approving authority
- CDSCO
- Product information
- ePatch 2.0 is indicated for use on patients who may be asymptomatic or who may suffer from transient symptoms such as shortness of breath, dizziness, light headedness, pre-syncope, syncope, fatigue, chest pain and/or anxiety. The ePatch 2.0 is intended for use by adolescents 18-21 and adults.
Holter Recorder [Electrocardio-gram Recorder] is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/001133_b5f89bb2e669fffab1561d46c0fc19dd_94a4fa8abe35f02ba61e922ce4b117b3. This device is marketed under the brand name ePatch. The license holder is PHILIPS INDIA LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.