RENASYS GO Canister - Indonesia BPOM Medical Device Registration
RENASYS GO Canister is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603026374. The device is manufactured by INTEGRA BIOTECHNICAL S.A.DE C.V (A SUBSIDIARY OF CARLISLE MEDICAL TECHNOLOGIES, LLC) from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BT. Encheval Putera Megatrading.
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
Country of Origin
Mexico
Authorized Representative
BT. Encheval Putera MegatradingAR Address
JL PULO LENTUT NO. 10 KWS INDUSTRI PULO GADUNG
Registration Date
May 31, 2024
Expiry Date
Dec 31, 2025
Product Type
Surgical Equipment
Surgical instrument motors and accessories/attachments.
Non Electromedic Non Sterile
OPHTEIS BIO 3.0
VSY BIYOTEKNOLOJI Ve IIac Sanayi Anonim Sirketi
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OPHTEIS FR Pro
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RENASYS-F Foam Dressing Kit with Soft Port (Harmac)
HARMAC MEDICAL PRODUCTS.
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SULCOFLEX TRIFOCAL
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OPHTEIS ORGANIC 1.8%
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