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FAMILY Dr. Pediatric Hernia Support - Indonesia BPOM Medical Device Registration

FAMILY Dr. Pediatric Hernia Support is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805220346. The device is manufactured by TAILIM CO. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOCORE PERKASA.

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BPOM Registered
Risk Class Kelas Resiko : A
FAMILY Dr. Pediatric Hernia Support
Analysis ID: AKL 10805220346

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

TAILIM CO.

Country of Origin

Korea

Authorized Representative

PT. INDOCORE PERKASA

AR Address

Komplek Graha Mas Pemuda Blok AB No. 19, Jl. Pemuda RT 020 / RW 006 Kel. Jati, Kec. Pulo Gadung, Jakarta Timur, DKI Jakarta

Registration Date

Sep 27, 2022

Expiry Date

Jun 26, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hernia support.

Non Electromedic Non Sterile

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