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GENADYNE Single Use Negative Pressure Wound Therapy Pump - Indonesia BPOM Medical Device Registration

GENADYNE Single Use Negative Pressure Wound Therapy Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603916919. The device is manufactured by GENADYNE BIOTECHNOLOGIES, INC., USA from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
GENADYNE Single Use Negative Pressure Wound Therapy Pump
Analysis ID: AKL 21603916919

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Oct 28, 2019

Expiry Date

Feb 01, 2024

Product Type

Surgical Equipment

Powered suction pump.

Non Radiation Electromedics

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