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NIPRO Luer Adapter - Indonesia BPOM Medical Device Registration

NIPRO Luer Adapter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902910656. The device is manufactured by NIPRO MEDICAL INDUSTRIES LTD. TATEBAYASI PLANT from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.

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
NIPRO Luer Adapter
Analysis ID: AKL 20902910656

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. MAIN WHEEL BEAM

AR Address

Perkantoran Duta Merlin Blok C No 58 jalan gajah mada

Registration Date

Oct 13, 2022

Expiry Date

Feb 17, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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