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DORNIER COMPACT DELTA II - Indonesia BPOM Medical Device Registration

DORNIER COMPACT DELTA II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805912179. The device is manufactured by DORNIER MEDTECH SYSTEMS GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PERMANA PUTRA MANDIRI.

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Risk Class Kelas Resiko : C
DORNIER COMPACT DELTA II
Analysis ID: AKL 20805912179

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. PERMANA PUTRA MANDIRI

AR Address

Jl. Taman Mini Indonesia Indah Pintu 2 atas No.43

Registration Date

May 08, 2023

Expiry Date

May 12, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Extracorporeal shock wave lithotripter.

Electromedic Radiation

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