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DK Filler Cannula - Indonesia BPOM Medical Device Registration

DK Filler Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902322441. The device is manufactured by YONG CHANG CO.,LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CAWANDRA JAYA 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
DK Filler Cannula
Analysis ID: AKL 20902322441

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

YONG CHANG CO.,LTD

Country of Origin

Korea

Authorized Representative

CAWANDRA JAYA INDONESIA

AR Address

Jalan Joe Kelapa Tiga 2A, Jagakarsa, Jakarta Selatan, Kel. Jagakarsa, Kec. Jagakarsa, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12520

Registration Date

Aug 22, 2023

Expiry Date

Apr 14, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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