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RUSCH Latex Rebreathing Bag - Indonesia BPOM Medical Device Registration

RUSCH Latex Rebreathing Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403912811. The device is manufactured by TELEFLEX MEDICAL SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : A. 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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BPOM Registered
Risk Class Kelas Resiko : A
RUSCH Latex Rebreathing Bag
Analysis ID: AKL 10403912811

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Malaysia

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Nov 06, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Anesthesia Equipment

Rebreathing device.

Non Electromedic Non Sterile

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