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JIBIMED WG SERIES PULSE VACUUM AUTOCLAVE - Indonesia BPOM Medical Device Registration

JIBIMED WG SERIES PULSE VACUUM AUTOCLAVE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903322208. The device is manufactured by JIANGYIN BINJIANG MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDIKA VISINDO PERKASA.

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
JIBIMED WG SERIES PULSE VACUUM AUTOCLAVE
Analysis ID: AKL 20903322208

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

MEDIKA VISINDO PERKASA

AR Address

Ruko Harmoni Blok HZ2 No.10 Harapan Indah Rt/Rw 11/16 Kel. Pusaka Rakyat Kec. Tarumajaya, Kota Bekasi, Jawa Barat 17214

Registration Date

Jul 18, 2023

Expiry Date

Aug 01, 2026

Product Type

General Hospital Equipment and Other Individuals

Steam sterilizer.

Non Radiation Electromedics

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