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SCHMITZ Patient Stretcher - Indonesia BPOM Medical Device Registration

SCHMITZ Patient Stretcher is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903125159. The device is manufactured by SCHMITZ U. SรถHNE GMBH & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is REDOSCO PRANA DIPTA.

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 : B
SCHMITZ Patient Stretcher
Analysis ID: AKL 20903125159

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

REDOSCO PRANA DIPTA

AR Address

Wangsa Niaga Wetan N0.15, Komplek Kota Baru Parahyangan

Registration Date

Aug 22, 2021

Expiry Date

Dec 31, 2024

Product Type

General Hospital Equipment and Other Individuals

Wheeled stretcher.

Non Electromedic Non Sterile

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