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Pasteur Pipette - India CDSCO Medical Device Registration

Pasteur Pipette is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000089_f430af6e7adb082b76967031958d776b_50c250fb9c260c079f3d2bc47c15f42c. This device is marketed under the brand name ESR. The license holder is Levram Lifesciences Pvt. Ltd., and it is classified as Device Class Class A. The approving authority is Dadra And Nagar Haveli.

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 A
Pasteur Pipette
UID: MFG/IVD/2022/000089_f430af6e7adb082b76967031958d776b_50c250fb9c260c079f3d2bc47c15f42c

Brand Name

ESR

Device Class

Class A

Approving Authority

Dadra And Nagar Haveli

Product Information

Pasteur Pipettes are intended for one-time use in handling and transferring liquid medical samples or analytes.

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