MYCLIP 2.0 Sectional Matrix Systems - Indonesia BPOM Medical Device Registration
MYCLIP 2.0 Sectional Matrix Systems is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603420307. The device is manufactured by POLYDENTIA SA from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.
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 : 1
Manufacturer
POLYDENTIA SACountry of Origin
Switzerland
Authorized Representative
PT. TAWADA HEALTHCAREAR Address
Rukan Permata Senayan Blok A18-19 Lantai 5 Jl. Tentara Pelajar No. 5
Registration Date
Aug 21, 2024
Expiry Date
May 31, 2029
Product Type
Surgical Dental Equipment
Dental hand instrument.
Non Electromedic Non Sterile
QUANTUM 2 (RF 12000)
SMITH & NEPHEW INC, ENDOSCOPY DIVISION
QUARTETโข Left Heart Lead
ABBOTT MEDICAL
ISOFLEX Lead
ABBOTT MEDICAL
SMITH & NEPHEW Fast Fix Instruments
ARTHROCARE CORPORATION
TWINFIX Ti Suture Anchors
ARTHROCARE CORPORATION
QUICKFLEXโข ยต Left Heart Lead
ABBOTT MEDICAL
HAETMED Small Steam Sterilizer
HAETMED (WUXI) CO., LTD.
SMITH & NEPHEW Genesis II Instrument
STRAITS ORTHOPAEDICS (MFG) SDN., BHD.
HAETMED Small Steam Sterilizer
HAETMED (WUXI) CO., LTD.
HAETMED Small Steam Sterilizer
HAETMED (WUXI) CO., LTD.

