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RUSCH Rectal Tube - Indonesia BPOM Medical Device Registration

RUSCH Rectal Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805712341. The device is manufactured by WILLY RUSCH GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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Risk Class Kelas Resiko : B
RUSCH Rectal Tube
Analysis ID: AKL 20805712341

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

WILLY RUSCH GMBH

Country of Origin

Germany

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Nov 10, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Gastroenterology-Urology Equipment

Colonic irrigation system.

Non Electromedic Non Sterile

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