Syntel® SIlicone Embolectomy Catheter - Regular Tip - Indonesia BPOM Medical Device Registration
Syntel® SIlicone Embolectomy Catheter - Regular Tip is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505220025. 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 GEM OF GRACE VIBRASA.
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
LEMAITRE VASCULAR, INCCountry of Origin
United States
Authorized Representative
GEM OF GRACE VIBRASAAR Address
Perkantoran CBD Ciledug Jl. Hos Cokroaminoto No. 93 Ruko perkantoran CBD Ciledug Blok A3 No. 28
Registration Date
Mar 21, 2022
Expiry Date
Apr 01, 2026
Product Type
Therapeutic Cardiology Equipment
Embolectomy catheter.
Non Electromedic Sterile
Pruitt Occlusion Catheter
PRUITT Irrigation Occlusion Catheter
PRUITT Aortic Occlusion Catheter
LEMAITRE VASCULAR Distal Perfusion Catheters
SYNTEL® SIlicone Embolectomy Catheter - Spring Tip
SYNTEL® Silicone Over the Wire Embolectomy Catheter
TUFTEX Over-the-Wire Embolectomy Catheter
OPI Hemostatic Forceps
BOTHWIN (BEIJING) MEDICAL TECHNOLOGY CO., LTD
HTKD Soft Tissue Retractor
BEIJING HANGTIAN KADI TECHNOLOGY R&D INSTITUTE
Pruitt Occlusion Catheter
LEMAITRE VASCULAR, INC
The OZAKI AVNeoTM Sizer System
DUMBBELL TECHNOLOGIES, INC

