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DENSSIFLO PTBD Catheter - Indonesia BPOM Medical Device Registration

DENSSIFLO PTBD Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420475. The device is manufactured by BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL 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 : C
DENSSIFLO PTBD Catheter
Analysis ID: AKL 20805420475

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. ANDAMAN MEDICAL INDONESIA

AR Address

Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma

Registration Date

Sep 12, 2024

Expiry Date

Mar 03, 2029

Product Type

Therapeutic Gastroenterology-Urology Equipment

Biliary catheter and accessories.

Non Electromedic Sterile

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