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GREATCARE Silicone Resuscitator - Indonesia BPOM Medical Device Registration

GREATCARE Silicone Resuscitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403516595. The device is manufactured by XIAMEN COMPOWER MEDICAL TECH. CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN SHADY.

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
GREATCARE Silicone Resuscitator
Analysis ID: AKL 20403516595

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MAIN SHADY

AR Address

Jalan Biak No. 33 C

Registration Date

Jul 07, 2023

Expiry Date

Jan 03, 2028

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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