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YIPAK Bowie Dick Test Pack - Indonesia BPOM Medical Device Registration

YIPAK Bowie Dick Test Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20901714132. The device is manufactured by ANQING YIPAK PACKAGING MATERIAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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
YIPAK Bowie Dick Test Pack
Analysis ID: AKL 20901714132

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

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

Nov 10, 2022

Expiry Date

Jun 14, 2027

Product Type

General and Individual Hospital Equipment Monitoring

Sterilization process indicator.

Non Electromedic Sterile

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