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ANMAKA ENDO STAPLER - Indonesia BPOM Medical Device Registration

ANMAKA ENDO STAPLER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421892. The device is manufactured by PRECISION CHANGZHOU MEDICAL INSTRUMENTS CO., LTD., from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANMAKA MAIN GROUP.

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BPOM Registered
Risk Class Kelas Resiko : C
ANMAKA ENDO STAPLER
Analysis ID: AKL 21603421892

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ANMAKA MAIN GROUP

AR Address

Jl. Carita no.190

Registration Date

Aug 20, 2024

Expiry Date

Aug 19, 2027

Product Type

Surgical Equipment

Implantable staple.

Non Electromedic Sterile

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