Philippines FDA registration CMDR-2024-02235

Heidi Mein Tourniquet 2 Channel with Printer

Philippines flagPhilippines·ATMOS MedizinTechnik GmbH & Co. KG Ludwig-Kegel-Straβe 16, 79853 Lenzkirch, Germany Mfd By: Ulrich GmbH & Co. KG - Buchbrunnenweg 12 89081 Ulm, Germany·Germany·Issued January 11, 2024 – January 11, 2029
Device information
Product Name
Heidi Mein Tourniquet 2 Channel with Printer
Registration Number
CMDR-2024-02235
Manufacturer details
Country of Origin
Germany
Importer & distribution
Importer/Distributor
Dubbel Medical Corporation
Registration dates
Issuance Date
January 11, 2024
Expiry Date
January 11, 2029
About this record

Access comprehensive regulatory information for Heidi Mein Tourniquet 2 Channel with Printer in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02235 and manufactured by ATMOS MedizinTechnik GmbH & Co. KG Ludwig-Kegel-Straβe 16, 79853 Lenzkirch, Germany Mfd By: Ulrich GmbH & Co. KG - Buchbrunnenweg 12 89081 Ulm, Germany in Germany. The device was registered on January 11, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Dubbel Medical 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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