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HEIL PHARMA Pro HP™ 2% - Indonesia BPOM Medical Device Registration

HEIL PHARMA Pro HP™ 2% is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203320408. The device is manufactured by HEIL PHARMA from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is DOCTOR PRO UTAMA.

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BPOM Registered
Risk Class Kelas Resiko : D
HEIL PHARMA Pro HP™ 2%

HEIL PHARMA Pro HPMC 2%

Analysis ID: AKL 31203320408

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

HEIL PHARMA

Country of Origin

India

Authorized Representative

DOCTOR PRO UTAMA

AR Address

PLAZA TAMAN HARAPAN BARU, BLOK D.2 LT.2 NOMOR 58, JALAN RAYA TAMAN HARAPAN BARU NOMOR 1

Registration Date

Oct 25, 2023

Expiry Date

May 31, 2026

Product Type

Surgical Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

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