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CALCIPAST Forte - Indonesia BPOM Medical Device Registration

CALCIPAST Forte is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602023434. The device is manufactured by PPH CERKAMED WOJCIECH PAWLOWSKI from Poland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. THOMASONG NIRMALA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
CALCIPAST Forte
Analysis ID: AKL 20602023434

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Poland

Authorized Representative

PT. THOMASONG NIRMALA

AR Address

JL. AM SANGAJI NO. 20A KEL. PETOJO UTARA, KEC. GAMBIR JAKARTA TELP. 021-63855888

Registration Date

Jun 23, 2020

Expiry Date

Mar 01, 2024

Product Type

Prosthetic Dental Equipment

Root canal filling resin

Non Electromedic Non Sterile

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