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EUROPCLIPS - Indonesia BPOM Medical Device Registration

EUROPCLIPS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420949. The device is manufactured by ACKERMANN INSTRUMENTE GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRANSMEDIC 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 : C
EUROPCLIPS
Analysis ID: AKL 21603420949

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

TRANSMEDIC INDONESIA

AR Address

Perkantoran Menara Era Unit G-01 JL.Senen Raya No.135-137 RT 00 RW 00, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Senen, Kel. Senen

Registration Date

May 02, 2024

Expiry Date

Dec 22, 2028

Product Type

Surgical Equipment

Implantable Clip

Non Electromedic Sterile

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