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PEDIALON Titanium Adapter - Indonesia BPOM Medical Device Registration

PEDIALON Titanium Adapter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220423. The device is manufactured by TIANJIN YOUWEI MEDICAL TREATMENT PLASTIC CORPORATION from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDI KHARISMA INTERNATIONAL.

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
PEDIALON Titanium Adapter
Analysis ID: AKL 20805220423

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDI KHARISMA INTERNATIONAL

AR Address

Jl. Darmo kali No.76, RT. 13/RW. 14 Kelurahan Darmo

Registration Date

Nov 09, 2022

Expiry Date

Aug 18, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Peritoneal dialysis system and accessories.

Non Electromedic Sterile

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