AnastoClip Atraumatic Forceps and Removers - Indonesia BPOM Medical Device Registration
AnastoClip Atraumatic Forceps and Removers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323941. The device is manufactured by LEMAITRE VASCULAR, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GEM OF GRACE VIBRASA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LEMAITRE VASCULAR, INC.Country of Origin
United States
Authorized Representative
PT. GEM OF GRACE VIBRASAAR Address
Ruko Perkantoran CBD Ciledug, Jl. HOS Cokroaminoto No. 93, Blok A3 No. 28-29, Kode Pos 15157, Kel. Karang Tengah, Kec. Karang Tengah, Kota Tangerang, Prov. Banten
Registration Date
Oct 31, 2023
Expiry Date
Apr 21, 2026
Product Type
Surgical Equipment
Implantable Clip
Non Electromedic Sterile
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