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Astringent Retraction Paste - India CDSCO Medical Device Registration

Astringent Retraction Paste is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000256_97f3bbea936d1515936d40158ac42237_92bb84e6715243fd8a9313c8b3751a3e. This device is marketed under the brand name Ketac Cem Radiopaque . The license holder is 3M 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.

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CDSCO Registered
Class Class B
Astringent Retraction Paste
UID: IMP/MD/2023/000256_97f3bbea936d1515936d40158ac42237_92bb84e6715243fd8a9313c8b3751a3e

Brand Name

Ketac Cem Radiopaque

License Holder

3M India Limited

Device Class

Class B

Approving Authority

CDSCO

Product Information

Astringent paste for temporary displacement of the marginal gingiva and for hemostasis and moisture control

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