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RIGIFLEX II Single Use Achalasia Balloon Dilator - Indonesia BPOM Medical Device Registration

RIGIFLEX II Single Use Achalasia Balloon Dilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805911311. The device is manufactured by CREGANNA MEDICAL S.R.L from Costa Rica, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BOSTON SCIENTIFIC 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.

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BPOM Registered
Risk Class Kelas Resiko : B
RIGIFLEX II Single Use Achalasia Balloon Dilator
Analysis ID: AKL 20805911311

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Costa Rica

Authorized Representative

PT. BOSTON SCIENTIFIC INDONESIA

AR Address

PRUDENTIAL TOWER, LT. 28, JL. JEND. SUDIRMAN KAV. 79

Registration Date

May 22, 2024

Expiry Date

Apr 07, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Gastrointestinal tube and accessories.

Non Electromedic Sterile

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