Herniotomy Instrument Set - Indonesia BPOM Medical Device Registration

Herniotomy Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103025637. The device is manufactured by PRECISA GMBH TOOLS from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEDICAL BLESSINGS OF THE ARCHIPELAGO.

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BPOM Registered

Risk Class Kelas Resiko : A

Herniotomy Instrument Set

Analysis ID: AKL 11103025637

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

PRECISA GMBH TOOLS

Country of Origin

Germany

Authorized Representative

MEDICAL BLESSINGS OF THE ARCHIPELAGO

AR Address

JALAN RUKAN SEDAYU SQUARE BLOK K-19, CENGKARENG

Registration Date

Sep 28, 2020

Expiry Date

Dec 11, 2024

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic general manual instrument.

Non Electromedic Non Sterile

DJ Fang

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