MEDUVENT Standard - Indonesia BPOM Medical Device Registration
MEDUVENT Standard is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403121399. The device is manufactured by WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALFA MEDIKA INDONESIA.
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.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Germany
Authorized Representative
PT. ALFA MEDIKA INDONESIAAR Address
RUKO BOULEVARD TEKNO BLOK AA NO. 11, RT011/001, JL. TEKNO WIDYA
Registration Date
Mar 27, 2024
Expiry Date
Mar 31, 2026
Product Type
Therapeutic Anesthesia Equipment
Powered emergency ventilator.
Non Radiation Electromedics
MEDUCORE Standard
WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG
ACCUVAC PRO
ATMOS MEDIZINTECHNIK GMBH & CO. KG
ACCUVAC LITE
ATMOS MEDIZINTECHNIK GMBH & CO. KG
MEDUCORE Standard 2
WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG
OXYWAY FAST II
WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG.
COMBIBAG Resuscitator
WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG
MEDUMAT Easy CPR
WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG
MEDUMAT STANDARD 2
WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG
MEDUMAT Transport
WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG
ERGON Variable Geometry Comfort Scoop Stretcher
ME. BER. SRL UNIPERSONALE

