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LAFOMED Autoclave - Indonesia BPOM Medical Device Registration

LAFOMED Autoclave is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903918386. The device is manufactured by NINGBO HAISHU LIFE MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ANDINI SARANA.

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
LAFOMED Autoclave
Analysis ID: AKL 20903918386

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ANDINI SARANA

AR Address

JL. Rawa Sumur III Kav. III Blok DD 11, Kawasan Industri Pulogadung

Registration Date

Jun 12, 2024

Expiry Date

Apr 19, 2029

Product Type

General Hospital Equipment and Other Individuals

Steam sterilizer.

Non Radiation Electromedics

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DJ Fang

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