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MulTipeg - Indonesia BPOM Medical Device Registration

MulTipeg is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10602320579. The device is manufactured by INTEGRATION DIAGNOSTICS SWEDEN AB from Sweden, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 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 : A
MulTipeg
Analysis ID: AKL 10602320579

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Sweden

Authorized Representative

THOMASONG NIRMALA

AR Address

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

Registration Date

May 15, 2023

Expiry Date

Jan 24, 2027

Product Type

Prosthetic Dental Equipment

Endosseous dental implant accessories.

Non Electromedic Non Sterile

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