Pure Global

Peha-haft - SFDA Registration ME0000001558SFDAA00386

Access comprehensive regulatory information for Peha-haft in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000001558SFDAA00386 and manufactured by PAUL HARTMANN AG.

This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.

Free Database
Powered by Pure Global AI
SFDA Official Data
Class I
ME0000001558SFDAA00386
Peha-haft
SFDA Registration: ME0000001558SFDAA00386
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Cohesive conforming bandage, latex free.

Product Use

For fixation bandaging and light compression.

Device Classification
Risk Class
Class I
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000001558SFDAA00386
Authorization ID
GHTF-2019-0446
Status
Active
Expire Date
December 22, 2020
Manufacturer
Manufacturer Name
PAUL HARTMANN AG
Model Information
Model ID(s)
932449 932444 932450 932445 932452 932446 932441 932447 932442 932448 932443
Product Accessories

[]