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D-LINE Triple Lumen ST Catheter Kits 13 French High Flow - Indonesia BPOM Medical Device Registration

D-LINE Triple Lumen ST Catheter Kits 13 French High Flow is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902410414. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
D-LINE Triple Lumen ST Catheter Kits 13 French High Flow
Analysis ID: AKL 20902410414

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

DIAN LANGGENG PRATAMA

AR Address

Jl. Raden Saleh Raya No. 4

Registration Date

Sep 14, 2022

Expiry Date

Jun 27, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Subcutaneous, implanted, intravascular infusion port and catheter.

Non Electromedic Sterile

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