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BAUSCH + LOMB RENU Fresh Multi-Purpose Solution - Indonesia BPOM Medical Device Registration

BAUSCH + LOMB RENU Fresh Multi-Purpose Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204410115. The device is manufactured by BAUSCH & LOMB INC, GREENVILLE SOLUTION PLANT from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BAUSCH LOMB INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
BAUSCH + LOMB RENU Fresh Multi-Purpose Solution
Analysis ID: AKL 21204410115

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BAUSCH LOMB INDONESIA

AR Address

Graha CIMB Niaga, Lt. 17, Jl. Jend. Sudirman Kav. 58

Registration Date

Oct 28, 2024

Expiry Date

Sep 29, 2027

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens care products.

Non Electromedic Sterile

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