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ENDO Single Use Sterile Specimen Pouch - Indonesia BPOM Medical Device Registration

ENDO Single Use Sterile Specimen Pouch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801320649. The device is manufactured by SURGAID MEDICAL (XIAMEN) CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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
ENDO Single Use Sterile Specimen Pouch
Analysis ID: AKL 20801320649

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Jul 17, 2023

Expiry Date

Feb 27, 2026

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Electromedic Sterile

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