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MEIBOMIAN Gland Evaluator - Indonesia BPOM Medical Device Registration

MEIBOMIAN Gland Evaluator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201127529. The device is manufactured by REMINGTON MEDICAL, S.A. from Dominican, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BRIDGE TWO.

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BPOM Registered
Risk Class Kelas Resiko : A
MEIBOMIAN Gland Evaluator
Analysis ID: AKL 11201127529

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Dominican

Authorized Representative

PT. BRIDGE TWO

AR Address

Petojo Melintang No. 17 Kel. Petojo Selatan, Kec. Gambir Jakarta Pusat

Registration Date

Dec 01, 2021

Expiry Date

Dec 31, 2024

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Electromedic Non Sterile

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