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THUASNE Lombastab Dorso - Indonesia BPOM Medical Device Registration

THUASNE Lombastab Dorso is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402122241. The device is manufactured by THUASNE from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BETWEEN PARTNERS OF SELF-SUFFICIENCY.

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Risk Class Kelas Resiko : A
THUASNE Lombastab Dorso
Analysis ID: AKL 11402122241

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

THUASNE

Country of Origin

France

AR Address

Jl. Pos Pengumben Raya No.8 RT.005 RW.005, Sukabumi Selatan, Kebon Jeruk, Jakarta Barat 11560

Registration Date

Jul 09, 2024

Expiry Date

May 13, 2029

Product Type

Prosthetic Physical Health Equipment

Truncal orthosis.

Non Electromedic Non Sterile

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