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ZKSK Endoscopic Gastrostomy (PEG) Kit - Indonesia BPOM Medical Device Registration

ZKSK Endoscopic Gastrostomy (PEG) Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420102. The device is manufactured by BEIJING ZKSK TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ENDO 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
ZKSK Endoscopic Gastrostomy (PEG) Kit
Analysis ID: AKL 20805420102

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Feb 19, 2024

Expiry Date

May 01, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Gastrointestinal tube and accessories.

Non Electromedic Sterile

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