Pure Global

PRIMAMED SWORD Herniotomy Instrument Set - Indonesia BPOM Medical Device Registration

PRIMAMED SWORD Herniotomy Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603912691. The device is manufactured by A SCHWEICKHARDT GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DAYA PRIMA MANDIRI JAYA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
PRIMAMED SWORD Herniotomy Instrument Set

PRIMAMED SCHWERT Herniotomy Instrument Set

Analysis ID: AKL 11603912691

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. DAYA PRIMA MANDIRI JAYA

AR Address

JL. KALIGARANG 1A SEMARANG

Registration Date

Jan 16, 2024

Expiry Date

Jan 15, 2027

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing