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ONEMED Amplatz Sheath - Indonesia BPOM Medical Device Registration

ONEMED Amplatz Sheath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420528. The device is manufactured by ASTER MEDISPRO PVT. LTD from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTIGLOBAL PERFECT RESULT SOURCE.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
ONEMED Amplatz Sheath
Analysis ID: AKL 20805420528

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. INTIGLOBAL PERFECT RESULT SOURCE

AR Address

KOMPLEK DARMO PARK II BLOK 4/14

Registration Date

Oct 17, 2024

Expiry Date

Oct 16, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Ureteral dilator.

Non Electromedic Sterile

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