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KENTAMED hARTT 400 - Indonesia BPOM Medical Device Registration

KENTAMED hARTT 400 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603718278. The device is manufactured by KENTAMED LTD. from Bulgaria, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FADZKURUNI.

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BPOM Registered
Risk Class Kelas Resiko : C
KENTAMED hARTT 400
Analysis ID: AKL 21603718278

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

KENTAMED LTD.

Country of Origin

Bulgaria

Authorized Representative

FADZKURUNI

AR Address

SALADDIN SQUARE BLOK B NO.23. JL. MARGONDA RAYA. PANCORAN MAS. KOTA DEPOK

Registration Date

Jan 25, 2024

Expiry Date

Jan 15, 2029

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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