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HENNISS Laparatomy Instrument Set - Indonesia BPOM Medical Device Registration

HENNISS Laparatomy Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10804110786. The device is manufactured by A. HENNISS. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MANDIRI JAYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : A
HENNISS Laparatomy Instrument Set
Analysis ID: AKL 10804110786

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

A. HENNISS.

Country of Origin

Germany

Authorized Representative

PT. MANDIRI JAYA MEDIKA

AR Address

Graha Mas Fatmawati Blok B No. 20, Jl. RS. Fatmawati No. 71

Registration Date

Apr 08, 2022

Expiry Date

Nov 08, 2026

Product Type

Gastroenterology-Surgical Urology Equipment

Manual gastroenterology-urology surgical instrument and accessories.

Non Electromedic Non Sterile

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