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MELAG Autoclave - Indonesia BPOM Medical Device Registration

MELAG Autoclave is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903112984. The device is manufactured by MELAG MEDIZINTECHNIK GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : B. 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 : B
MELAG Autoclave
Analysis ID: AKL 20903112984

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. THOMASONG NIRMALA

AR Address

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

Registration Date

Nov 25, 2020

Expiry Date

Jun 30, 2025

Product Type

General Hospital Equipment and Other Individuals

Steam sterilizer.

Non Radiation Electromedics

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