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ZIMMER BIOMET 12/14 Head Trials - Indonesia BPOM Medical Device Registration

ZIMMER BIOMET 12/14 Head Trials is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303022890. 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 BIOMET 12/14 Head Trials
Analysis ID: AKL 11303022890

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.TAMAN MINI PINTU 2 NO. 2, RT. 006 RW. 004

Registration Date

Sep 06, 2024

Expiry Date

Dec 08, 2026

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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