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HUGEMED SINGLE USE CYSTOSCOPE - Indonesia BPOM Medical Device Registration

HUGEMED SINGLE USE CYSTOSCOPE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420417. The device is manufactured by SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD., from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ADMIRAL BLESENSA IMMORTAL.

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BPOM Registered
Risk Class Kelas Resiko : B
HUGEMED SINGLE USE CYSTOSCOPE
Analysis ID: AKL 20801420417

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ADMIRAL BLESENSA IMMORTAL

AR Address

Ruko Graha Handaya unit H Jl. Raya Pejuangan Kav. 12A, Kebon Jeruk, Kota Jakarta Barat, Kode Pos 11530

Registration Date

Nov 25, 2024

Expiry Date

May 22, 2027

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Electromedic Sterile

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