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BIOTEQ Ureteral Stent Set - Indonesia BPOM Medical Device Registration

BIOTEQ Ureteral Stent Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804420060. The device is manufactured by BIOTEQUE CORPORATION I-LAN FACTORY II from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INTIGLOBAL PERFECT RESULT SOURCE.

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BPOM Registered
Risk Class Kelas Resiko : C
BIOTEQ Ureteral Stent Set
Analysis ID: AKL 20804420060

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. INTIGLOBAL PERFECT RESULT SOURCE

AR Address

KOMPLEK DARMO PARK II BLOK 4/14

Registration Date

Apr 29, 2024

Expiry Date

Mar 31, 2026

Product Type

Gastroenterology-Surgical Urology Equipment

Ureteral stent.

Non Electromedic Sterile

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