Pure Global

FIEGERT-ENDOTECH Arthroscopy Shaver Blades Standard with Plastic Coupler - Indonesia BPOM Medical Device Registration

FIEGERT-ENDOTECH Arthroscopy Shaver Blades Standard with Plastic Coupler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303311980. The device is manufactured by FIEGERT ENDOTECH MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIMARY WORKS.

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
FIEGERT-ENDOTECH Arthroscopy Shaver Blades Standard with Plastic Coupler
Analysis ID: AKL 11303311980

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. PRIMARY WORKS

AR Address

Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper

Registration Date

Oct 14, 2021

Expiry Date

Nov 27, 2025

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing