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NEOTECH NeoSeal - Indonesia BPOM Medical Device Registration

NEOTECH NeoSeal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20404220049. The device is manufactured by NEOTECH PRODUCTS LLC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDRA PRIMA JAYA.

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
NEOTECH NeoSeal
Analysis ID: AKL 20404220049

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. ANDRA PRIMA JAYA

AR Address

JL. TANAH ABANG III NO. 19E KEL. PETOJO SELATAN KEC. GAMBIR

Registration Date

Dec 08, 2022

Expiry Date

Dec 31, 2025

Product Type

Other Anesthesia Equipment

Nose clip.

Non Electromedic Non Sterile

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