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AESCULAP Abdominal Surgery Instrument - Indonesia BPOM Medical Device Registration

AESCULAP Abdominal Surgery Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10804900185. The device is manufactured by AESCULAP AG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
AESCULAP Abdominal Surgery Instrument
Analysis ID: AKL 10804900185

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

AESCULAP AG.

Country of Origin

Germany

Authorized Representative

B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Dec 15, 2024

Expiry Date

Mar 01, 2027

Product Type

Gastroenterology-Surgical Urology Equipment

Manual gastroenterology-urology surgical instrument and accessories.

Non Electromedic Sterile

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