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VBM Silicone Resuscitator Set - Indonesia BPOM Medical Device Registration

VBM Silicone Resuscitator Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220150. The device is manufactured by VBM MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDONESIAN MEDICAL INNOVATION.

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
VBM Silicone Resuscitator Set
Analysis ID: AKL 20403220150

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. INDONESIAN MEDICAL INNOVATION

AR Address

BizPark 3 Bekasi, Blok D 60A Kalibaru Kec. Medan Satria, Kota Bekasi, Jawa Barat, 17132

Registration Date

Nov 20, 2024

Expiry Date

Dec 31, 2027

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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