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E-LIFE FOAM CERVICAL COLLAR - Indonesia BPOM Medical Device Registration

E-LIFE FOAM CERVICAL COLLAR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402024980. The device is manufactured by ZHANG PU ORTHOLIFE REHABILITATION CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SAPTA MANDIRI INDONESIA.

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
E-LIFE FOAM CERVICAL COLLAR
Analysis ID: AKL 11402024980

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SAPTA MANDIRI INDONESIA

AR Address

Rukan Exclusive Radin Inten, Kav 23. Jl. Radin Inten II No 80

Registration Date

Oct 22, 2024

Expiry Date

Jul 25, 2029

Product Type

Prosthetic Physical Health Equipment

Truncal orthosis.

Non Electromedic Non Sterile

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