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SMARTVISC Viscoelastic Solution Set for Intraocular Use - Indonesia BPOM Medical Device Registration

SMARTVISC Viscoelastic Solution Set for Intraocular Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203810539. The device is manufactured by RUMEX INTERNATIONAL LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. PANCARAYA KRISNAMANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : D
SMARTVISC Viscoelastic Solution Set for Intraocular Use
Analysis ID: AKL 31203810539

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United Kingdom

Authorized Representative

PT. PANCARAYA KRISNAMANDIRI

AR Address

KOMPLEK FATMAWATI MAS BLOK II KAV. 228/229, JALAN TEROGONG RAYA

Registration Date

Aug 27, 2021

Expiry Date

Jun 01, 2026

Product Type

Surgical Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

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