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NOVOFINE Plus , 32G 4mm - Indonesia BPOM Medical Device Registration

NOVOFINE Plus , 32G 4mm is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220911. The device is manufactured by NEW NORDISK A/S from Denmark, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ANUGRAH ARGON MEDICA.

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BPOM Registered
Risk Class Kelas Resiko : B
NOVOFINE Plus , 32G 4mm
Analysis ID: AKL 20902220911

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

NEW NORDISK A/S

Country of Origin

Denmark

Authorized Representative

ANUGRAH ARGON MEDICA

AR Address

Titan Center Lantai 4, Jl. Boulevard Bintaro Blok B7/B1 No. 5 Bintaro Jaya Sektor 7

Registration Date

Dec 30, 2024

Expiry Date

Mar 31, 2029

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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