SupraFelt Cartilage Repair - Indonesia BPOM Medical Device Registration
SupraFelt Cartilage Repair is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420144. The device is manufactured by BMT CALSIS HEALTH TECHNOLOGIES SAN. TIC. AS from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EUFRAT WITH.
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
BMT CALSIS HEALTH TECHNOLOGIES SAN. TIC. ASCountry of Origin
Turkey
Authorized Representative
EUFRAT WITHAR Address
Ruko Gardenia kav 1, jln. parigi raya no 75 sukabakti curug 15810
Registration Date
Apr 24, 2024
Expiry Date
Oct 02, 2028
Product Type
Prosthetic Orthopedic Equipment
Single/multiple component metallic bone fixation appliances and accessories.
Non Electromedic Sterile
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