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RUSCH – Crystal Clear Tracheostomy Cannula - Indonesia BPOM Medical Device Registration

RUSCH – Crystal Clear Tracheostomy Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403914097. The device is manufactured by TELEFLEX MEDICAL SDN BHD from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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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Risk Class Kelas Resiko : B
RUSCH – Crystal Clear Tracheostomy Cannula
Analysis ID: AKL 20403914097

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Oct 14, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Anesthesia Equipment

Tracheostomy tube and tube cuff.

Non Electromedic Sterile

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