Drug-coated peripheral angioplasty balloon - Vietnam Registration 55900
Access comprehensive regulatory information for Drug-coated peripheral angioplasty balloon in Vietnam's medical device market through Pure Global AI's free database. is registered under number 55900 and manufactured by LUTONIX , INC. USA. The authorized representative in Vietnam is Dk Medical Company Limited.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Aesculap Chifa Sp. z o. o., Eucatech AG, 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 18 2.5 x 120 mm 130 cm)
SEQUENT PLEASE OTW 18 2.5 x 120 mm 130 cm
Aesculap Chifa Sp. z o. o.
469142
Drug-coated peripheral angioplasty balloon (SeQuent PLEASE OTW 18 3 x 40 mm 130 cm)
SEQUENT PLEASE OTW 18 3 x 40 mm 130 cm
Aesculap Chifa Sp. z o. o.
469143
Drug-coated peripheral angioplasty balloon (SeQuent PLEASE OTW 18 6 x 80 mm 75 cm)
SEQUENT PLEASE OTW 18 6 x 80 mm 75 cm
Aesculap Chifa Sp. z o. o.
469135
Drug-coated peripheral angioplasty balloon (SeQuent PLEASE OTW 18 3.5 x 120 mm 130 cm)
SEQUENT PLEASE OTW 18 3.5 x 120 mm 130 cm
Aesculap Chifa Sp. z o. o.
469148

