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FORSCH MEDICAL Foley Catheter - Indonesia BPOM Medical Device Registration

FORSCH MEDICAL Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220110. The device is manufactured by GUANGDONG ECAN MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DWIASRI GRAHA.

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 : C
FORSCH MEDICAL Foley Catheter
Analysis ID: AKL 20805220110

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DWIASRI GRAHA

AR Address

Jalan Utan Kayu Raya Nomor 19 A, Desa/Kelurahan Utan Kayu Utara, Kec. Matraman, Kota Adm. Jakarta Timur, Provinsi DKI Jakarta, Kode Pos: 13120

Registration Date

Nov 12, 2024

Expiry Date

Nov 12, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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