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GENADYNE Nanogen Actigel - Indonesia BPOM Medical Device Registration

GENADYNE Nanogen Actigel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420799. The device is manufactured by GENADYNE BIOTECHNOLOGIES, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SEKARGUNA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
GENADYNE Nanogen Actigel

GENADYNE Nanogen Aktigel

Analysis ID: AKL 21603420799

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

SEKARGUNA MEDIKA

AR Address

JL. Ciputat Raya Nomor 64

Registration Date

Apr 06, 2024

Expiry Date

May 23, 2028

Product Type

Surgical Equipment

Hydrogel wound dressing and burn dressing.

Non Electromedic Sterile

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