ORTHOPLUS Neoprene Shoulder Support - Indonesia BPOM Medical Device Registration

ORTHOPLUS Neoprene Shoulder Support is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402420476. The device is manufactured by ZHANGPU ORTHOLIFE REHABILITATION CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ORTHOCARE INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : A

ORTHOPLUS Neoprene Shoulder Support

Analysis ID: AKL 11402420476

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

ZHANGPU ORTHOLIFE REHABILITATION CO.,LTD.

Country of Origin

China

Authorized Representative

PT. ORTHOCARE INDONESIA

AR Address

Ruko Galeri Niaga Mediterania 2 Blok N 8 J, Jalan Pantai Indah Utara II Rt/Rw : 007/008

Registration Date

Nov 14, 2024

Expiry Date

May 15, 2029

Product Type

Prosthetic Physical Health Equipment

Prosthetic and orthotic accessory.

Non Electromedic Non Sterile

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ORTHOPLUS Neoprene Shoulder Support

ZHANG PU ORTHOPLIFE REHABILITATION CO., LTD.

ORTHOPLUS Neoprene Shoulder Support - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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ORTHOPLUS Neoprene Shoulder Support

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