Pure Global

SYMMETRY MEDICAL Revisions Solutions - Indonesia BPOM Medical Device Registration

SYMMETRY MEDICAL Revisions Solutions is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303320392. The device is manufactured by SYMMETRY MEDICAL MANUFACTURING INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. JOHNSON AND JOHNSON INDONESIA TWO.

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
SYMMETRY MEDICAL Revisions Solutions
Analysis ID: AKL 11303320392

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. JOHNSON AND JOHNSON INDONESIA TWO

AR Address

K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A, Kuningan, Setiabudi, Jakarta Selatan

Registration Date

Sep 23, 2024

Expiry Date

Apr 21, 2028

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