HILL-ROM Accella Therapy - Indonesia BPOM Medical Device Registration

HILL-ROM Accella Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902020898. The device is manufactured by HILL-ROM S.A.S from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS 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 : B

HILL-ROM Accella Therapy

Analysis ID: AKL 20902020898

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

Country of Origin

France

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Oct 07, 2024

Expiry Date

Dec 31, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Alternating pressure air flotation mattress.

Non Radiation Electromedics

DJ Fang

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Other Products from HILL-ROM S.A.S

Products from the same manufacturer (3 products)

Hill-Rom® 900

Kelas Resiko : B

HILL-ROM® 900 Accella ™ Bed

Kelas Resiko : B

HILL-ROM® 900

Kelas Resiko : B

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