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AMD Tyvek Sterilization Reel Pouch - Indonesia BPOM Medical Device Registration

AMD Tyvek Sterilization Reel Pouch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903322377. The device is manufactured by NANTONG FUHUA MEDICAL PACKING CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CIPTA MEDIKA 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
AMD Tyvek Sterilization Reel Pouch
Analysis ID: AKL 20903322377

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. CIPTA MEDIKA INDONESIA

AR Address

Grand Unedo, Jl. Raya Bina Warga No.94 G, RT.006 RW.002, Kelurahan Cipayung, Kecamatan Cipayung, Jakarta Timur, DKI Jakarta

Registration Date

Sep 02, 2023

Expiry Date

Jun 21, 2027

Product Type

General Hospital Equipment and Other Individuals

Sterilization wrap.

Non Electromedic Non Sterile

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