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STERiJECT Hypodermic Needle - Indonesia BPOM Medical Device Registration

STERiJECT Hypodermic Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221245. The device is manufactured by TSK LABORATORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
STERiJECT Hypodermic Needle
Analysis ID: AKL 20902221245

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TSK LABORATORY

Country of Origin

Japan

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan

Registration Date

Oct 06, 2023

Expiry Date

Jun 15, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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