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3DMED TiNAiLab - Indonesia BPOM Medical Device Registration

3DMED TiNAiLab is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220418. The device is manufactured by 3D BIOMEDICINE SCIENCE & TECHNOLOGY, CO., LIMITED from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTERSKALA MEDIKA 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
3DMED TiNAiLab
Analysis ID: AKL 21501220418

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INTERSKALA MEDIKA INDONESIA

AR Address

Green Sedayu Biz Park Blok DM 9/62, Jalan Daan Mogot Km.18

Registration Date

Sep 02, 2022

Expiry Date

Jun 29, 2027

Product Type

Diagnostic Radiology Equipment

(Dihapus) Picture archiving and communications system.

Non Radiation Electromedics

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