MAXBRAID PE Suture - Indonesia BPOM Medical Device Registration
MAXBRAID PE Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603022993. The device is manufactured by TELEFLEX MEDICAL DE MEXICO, S. DE R.L. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TELEFLEX MEDICAL DE MEXICO, S. DE R.L. DE C.V.Country of Origin
Mexico
Authorized Representative
PT. KALMED SEJAHTERA INDONESIAAR Address
Jl. TMII Pintu II No. 2, RT 006 RW 004,
Registration Date
May 29, 2020
Expiry Date
Nov 11, 2024
Product Type
Surgical Equipment
Nonabsorbable poly(ethylene terephthalate) surgical suture.
Non Electromedic Sterile
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