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VYGON Umbilical Catheter - Indonesia BPOM Medical Device Registration

VYGON Umbilical Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902318253. The device is manufactured by VYGON from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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Risk Class Kelas Resiko : C
VYGON Umbilical Catheter
Analysis ID: AKL 20902318253

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

VYGON

Country of Origin

France

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Dec 23, 2022

Expiry Date

Dec 31, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular catheter.

Non Electromedic Sterile

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