Full Echo 23cm - Indonesia BPOM Medical Device Registration
Full Echo 23cm is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105023030. The device is manufactured by LABORATOIRE CCD from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is NUGRA KARSERA.
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
LABORATOIRE CCDCountry of Origin
France
Authorized Representative
NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Jun 02, 2020
Expiry Date
Dec 31, 2023
Product Type
Reproductive Aids
Assisted reproduction catheters.
Non Electromedic Sterile
FRYDMAN Classic
CCD SET TDT
OPS with Valve Tube 100 Needle 35cm G17
OPS without Valve Tube 100 Needle 35cm G17
Pearl Tip Classic
Pearl Tip Soft
LABORATOIRE Full Echo Pro
Seren AND
TACTICATH™ Contact Force Ablation Catheter, Sensor Enabled™
ABBOTT MEDICAL
Z-MED II ™ Percutaneous Transluminal Valvulopasty Catheter
NUMED INC.
NUCLEUS Percutaneous Transluminal Valvuloplasty Catheter
NUMED, INC.
TYSHAK Mini Pediatric Valvuloplasty Catheter
NUMED, INC.
Z-5 ™ Atrioseptostomy Catheter
NUMED INC.
TYSHAK Percutaneous Transluminal Valvuloplasty Catheter
NUMED, INC.
Fast Cath ™ Hemostasis Introducer
ABBOTT MEDICAL
SWARTZ ™ Braided Transseptal Guiding Introducer
ABBOTT MEDICAL
Ensite Precision ™ Surface Electrode Kit
ABBOTT MEDICAL COSTA RICA LTDA.
TYSHAK II Percutaneous Valvuloplasty Catheter
NUMED, INC.