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BD Ultra-Fine ™ PRO - Indonesia BPOM Medical Device Registration

BD Ultra-Fine ™ PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902911308. The device is manufactured by BECTON DICKINSON AND COMPANY from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BECTON DICKINSON INDONESIA.

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
BD Ultra-Fine ™ PRO
Analysis ID: AKL 20902911308

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Ireland

Authorized Representative

BECTON DICKINSON INDONESIA

AR Address

SAMPOERNA STRATEGIC SQUARE, SOUTH TOWER LT.20 JL. JEND SUDIRMAN KAV 45-46

Registration Date

Aug 15, 2023

Expiry Date

Nov 29, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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