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FEELject Soft Micro Cannula - Indonesia BPOM Medical Device Registration

FEELject Soft Micro Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902421486. The device is manufactured by FEEL-TECH CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INSIGHTOF CONSULTING INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
FEELject Soft Micro Cannula
Analysis ID: AKL 20902421486

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

FEEL-TECH CO., LTD

Country of Origin

Korea

Authorized Representative

PT. INSIGHTOF CONSULTING INDONESIA

AR Address

Jalan Amil RT.3/RW.4 Nomor 3A

Registration Date

Dec 30, 2024

Expiry Date

Jun 24, 2029

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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