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AESCULAP Atraumata Clamps - Indonesia BPOM Medical Device Registration

AESCULAP Atraumata Clamps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603900046. The device is manufactured by AESCULAP AG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is B. BRAUN MEDICAL 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 : A
AESCULAP Atraumata Clamps
Analysis ID: AKL 11603900046

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

AESCULAP AG.

Country of Origin

Germany

Authorized Representative

B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Oct 10, 2022

Expiry Date

Nov 18, 2026

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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