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ZIMMER Multipolar Bipolar Instruments - Indonesia BPOM Medical Device Registration

ZIMMER Multipolar Bipolar Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303915386. The device is manufactured by ZIMMER INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
ZIMMER Multipolar Bipolar Instruments
Analysis ID: AKL 11303915386

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

ZIMMER INC.

Country of Origin

United States

Authorized Representative

PT. KALMED SEJAHTERA INDONESIA

AR Address

Jl. TMII Pintu II No. 2, RT 006 RW 004,

Registration Date

Apr 20, 2022

Expiry Date

Dec 08, 2026

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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