Peripheral angioplasty balloon - Vietnam Registration 25918
Access comprehensive regulatory information for Peripheral angioplasty balloon in Vietnam's medical device market through Pure Global AI's free database. is registered under number 25918 and manufactured by Lake Region Medical. The authorized representative in Vietnam is Medtronic Vietnam Company Limited.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including ev3, Inc., Medtronic Mexico S.de R.L.de CV, and 5 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Drug-coated peripheral angioplasty balloon (SeQuent PLEASE OTW 18 5 x 80 mm 75 cm)
SEQUENT PLEASE OTW 18 5 x 80 mm 75 cm
Aesculap Chifa Sp. z o. o.
469131
Drug-coated peripheral angioplasty balloon (SeQuent PLEASE OTW 35 4.0 x 60 mm 130 cm)
SeQuent PLEASE OTW 35 4.0 x 60 mm 130 cm
Aesculap Chifa Sp. z o. o.
337103
Drug-coated peripheral angioplasty balloon (SeQuent PLEASE OTW 35 6.0 x 150 mm 75 cm)
SeQuent PLEASE OTW 35 6.0 x 150 mm 75 cm
Aesculap Chifa Sp. z o. o.
337097
Peripheral angioplasty balloon coated with Paclitaxel
Lutonix 014 Drug Coated Balloon PTA Catheter
Lutonix, Inc
329287
Peripheral angioplasty balloon
Bóng nong ngoại biên dùng cho can thiệp nong cầu nối loại Perseus-q 18 Dialysis Fistulae
QualiMed Innovative Medizinprodukte GmbH
161455