Pure Global

TONTARRA Laparotomy Instrument Set - Indonesia BPOM Medical Device Registration

TONTARRA Laparotomy Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10804917496. The device is manufactured by TONTARRA MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEDTEK.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
TONTARRA Laparotomy Instrument Set
Analysis ID: AKL 10804917496

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

MEDTEK

AR Address

Delta Building, Blok A-11, C-1 dan C-2, Jl. Suryopronoto No. 1-9

Registration Date

Oct 06, 2022

Expiry Date

Aug 30, 2027

Product Type

Gastroenterology-Surgical Urology Equipment

Manual gastroenterology-urology surgical instrument and accessories.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing