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SAMPLIX TUBE LH LITHIUM HEPARIN SEPARATOR 13X75 LIGHT GREEN CAP, NON-RIDGED' - FDA Registration MDR-08084

Access comprehensive regulatory information for SAMPLIX TUBE LH LITHIUM HEPARIN SEPARATOR 13X75 LIGHT GREEN CAP, NON-RIDGED' in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08084 and manufactured by Greiner Bio-One GmbH in Thailand. The device was registered on April 01, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Andaman Medical Philippines 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.

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Thailand
MDR-08084
SAMPLIX TUBE LH LITHIUM HEPARIN SEPARATOR 13X75 LIGHT GREEN CAP, NON-RIDGED'
Registered medical device in Philippines
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Device Information
Product Name
SAMPLIX TUBE LH LITHIUM HEPARIN SEPARATOR 13X75 LIGHT GREEN CAP, NON-RIDGED'
Registration Number
MDR-08084
Manufacturer Details
Country of Origin
Thailand
Importer & Distribution
Registration Dates
Issuance Date
April 01, 2020
Expiry Date
May 09, 2025