PICO SINGLE USE NEGATIVE PRESSURE WOUND THERAPY SYSTEM - FDA Registration MDR-09938
Access comprehensive regulatory information for PICO SINGLE USE NEGATIVE PRESSURE WOUND THERAPY SYSTEM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09938 and manufactured by Smith & Nephew Pte. Ltd. in England. The device was registered on July 08, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (East Lane Corporation), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.
Free Database
Powered by Pure Global AI
FDA Official Data
England
MDR-09938
PICO SINGLE USE NEGATIVE PRESSURE WOUND THERAPY SYSTEM
Registered medical device in Philippines
Device Information
Product Name
PICO SINGLE USE NEGATIVE PRESSURE WOUND THERAPY SYSTEM
Registration Number
MDR-09938
Manufacturer Details
Manufacturer
Smith & Nephew Pte. Ltd.Country of Origin
England
Importer & Distribution
Importer/Distributor
East Lane CorporationRegistration Dates
Issuance Date
July 08, 2020
Expiry Date
July 08, 2021

