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BD Ultra-Fine™ Insulin Syringes - Indonesia BPOM Medical Device Registration

BD Ultra-Fine™ Insulin Syringes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420318. The device is manufactured by BD MEDICAL DIABETES CARE from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.

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™ Insulin Syringes
Analysis ID: AKL 20902420318

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Dec 30, 2024

Expiry Date

Jan 03, 2029

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Electromedic Sterile

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