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REPLACEMENT PEG TUBE - India CDSCO Medical Device Registration

REPLACEMENT PEG TUBE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000013_df699a0b90260d1c793741d52ba6bcc0_ce70a6a5ff524a00ee1803d45739c467. This device is marketed under the brand name ENDOTRECS. The license holder is Medinova Endosys, and it is classified as Device Class Class B. The approving authority is Gujarat.

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
REPLACEMENT PEG TUBE
UID: MFG/MD/2021/000013_df699a0b90260d1c793741d52ba6bcc0_ce70a6a5ff524a00ee1803d45739c467

Brand Name

ENDOTRECS

License Holder

Medinova Endosys

Device Class

Class B

Approving Authority

Gujarat

Product Information

used for percutaneous endoscopic gastrostomy placement to provide enteral nutrition to patient requiring nutritional support

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