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Umbilical Catheter - India CDSCO Medical Device Registration

Umbilical Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000148_ac5ec61de32aa78bfb23becaa527d3c8_4f22110064429533c24cdd331601cc15. This device is marketed under the brand name Dermafilm & Dermincise. The license holder is VYGON INDIA PRIVATE 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.

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CDSCO Registered
Class Class B
Umbilical Catheter
UID: IMP/MD/2019/000148_ac5ec61de32aa78bfb23becaa527d3c8_4f22110064429533c24cdd331601cc15

Brand Name

Dermafilm & Dermincise

Device Class

Class B

Approving Authority

CDSCO

Product Information

Catheter inserted in the umbilical vein or in the umbilical artery of the newborn. Umbilical venous catheter are used in case of neonatal emergency, for a short period of time (Dermafilm & Dermincise). It allows: the infusion of parenteral nutrition, the administration of drugs, exchange - transfusion...) The umbilical arterial catheter is used in case of neonatal emergency for blood gas monitoring, blood pressure measurement

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