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REMEDI Endotracheal Tube With Cuffed - Indonesia BPOM Medical Device Registration

REMEDI Endotracheal Tube With Cuffed is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403312412. The device is manufactured by HOSPITAL & HOMECARE IMP & EXP. CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANUGRAHMITRA SELARAS.

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BPOM Registered
Risk Class Kelas Resiko : B
REMEDI Endotracheal Tube With Cuffed
Analysis ID: AKL 20403312412

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ANUGRAHMITRA SELARAS

AR Address

Jl. Agung Niaga IV Blok G.4 No. 54 Kel. Sunter Agung, Kec. Tanjung Priok, Jakarta Utara

Registration Date

Jun 13, 2023

Expiry Date

Mar 04, 2026

Product Type

Therapeutic Anesthesia Equipment

Tracheal tube.

Non Electromedic Sterile

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