Pure Global

3M STERI-DRAPE Patient Isolation Drape - Indonesia BPOM Medical Device Registration

3M STERI-DRAPE Patient Isolation Drape is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422626. The device is manufactured by 3M EDUMEX S.A DE C.V from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BRIDGE TWO.

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 : B
3M STERI-DRAPE Patient Isolation Drape
Analysis ID: AKL 21603422626

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Nov 10, 2024

Expiry Date

Mar 22, 2029

Product Type

Surgical Equipment

Surgical drape and drape accessories.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing