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FIGULLA Flex II ASD Occluder - Indonesia BPOM Medical Device Registration

FIGULLA Flex II ASD Occluder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503719276. The device is manufactured by OCCLUTECH GMBH. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : D
FIGULLA Flex II ASD Occluder
Analysis ID: AKL 30503719276

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

OCCLUTECH GMBH.

Country of Origin

Germany

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Feb 22, 2023

Expiry Date

Dec 13, 2027

Product Type

Prosthetic Cardiology Equipment

Cardiac occluder

Non Electromedic Sterile

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