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BD 20mL Syringe - Indonesia BPOM Medical Device Registration

BD 20mL Syringe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220654. The device is manufactured by BECTON DICKINSON AND COMPANY from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 20mL Syringe
Analysis ID: AKL 20902220654

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BECTON DICKINSON INDONESIA

AR Address

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

Registration Date

Dec 23, 2023

Expiry Date

Feb 15, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Electromedic Sterile

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