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JOLINE Smooth Flow Double Lumen LT - Indonesia BPOM Medical Device Registration

JOLINE Smooth Flow Double Lumen LT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805321094. The device is manufactured by JOLINE GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DIAN LANGGENG PRATAMA.

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
JOLINE Smooth Flow Double Lumen LT
Analysis ID: AKL 20805321094

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

DIAN LANGGENG PRATAMA

AR Address

Gedung Dinar, Jl. Raden Saleh Raya No. 4 RT.10/RW.01, Kel. Kenari, Kec. Senen. Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos 10430

Registration Date

Dec 29, 2023

Expiry Date

Jul 06, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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