SIDAPHARM Sterile Ophthalmic Drape - Indonesia BPOM Medical Device Registration
SIDAPHARM Sterile Ophthalmic Drape is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603710320. The device is manufactured by SIDAPHARM P.C. from Greece, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIUMPHANT MANDARIN OPTO-MEDIC.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
SIDAPHARM P.C.Country of Origin
Greece
Authorized Representative
PT. TRIUMPHANT MANDARIN OPTO-MEDICAR Address
Jl. Senen Raya No. 135 Ruko Atrium Blok C No. 15 Jakarta Pusat 10410 Tlp : 021-3515478, 3516018 Fax : 021-3511606
Registration Date
Mar 10, 2023
Expiry Date
Dec 23, 2026
Product Type
Surgical Equipment
Surgical drape and drape accessories.
Non Electromedic Sterile
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SIDA-HPMC 2% Hydroxypropyl Methylcellulose Opthalmic Solution
SIDA-LENS Hydrophilic Onepiece Acrylic Foldable Intraocular Lens
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SIDAPHARM Ophthalmic Micro Surgical Cannulas
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SIDA-VISC 1.8% Sodium Hyaluronate Opthalmic Solution
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SIDA-LENS PMMA Intraocular Lens
MOCHINTRA DIANA SIDAPHARM GREECE
SIDA-HPMC 2% Hydroxypropyl Methylcellulose Opthalmic Solution
SIDAPHARM P.C.

