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LA-MED IV Infusion Set with Air Vented - Indonesia BPOM Medical Device Registration

LA-MED IV Infusion Set with Air Vented is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902918903. The device is manufactured by LA-MED HEALTHCARE PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KASTARA TECHNOLOGY INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : C
LA-MED IV Infusion Set with Air Vented
Analysis ID: AKL 20902918903

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. KASTARA TECHNOLOGY INTERNATIONAL

AR Address

Ifolia HY.47 No. 43 RT 02 RW 20 Harapan Indah

Registration Date

Jul 02, 2024

Expiry Date

Feb 06, 2029

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

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