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GENSUFINE ™ Pen Needles - Indonesia BPOM Medical Device Registration

GENSUFINE ™ Pen Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902912451. The device is manufactured by KD MEDICAL GMBH HOSPITAL PRODUCTS from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
GENSUFINE ™ Pen Needles
Analysis ID: AKL 20902912451

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. UBC MEDICAL INDONESIA

AR Address

Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930

Registration Date

Apr 22, 2019

Expiry Date

Feb 14, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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