Philippines FDA registration MDR-01601
VENOFIX® SAFETY WINGED IV NEEDLE
Device information
- Product Name
- VENOFIX® SAFETY WINGED IV NEEDLE
- Registration Number
- MDR-01601
Manufacturer details
- Manufacturer
- B. Braun Melsungen AG
- Country of Origin
- Malaysia
Importer & distribution
- Importer/Distributor
- B. Braun Medical Supplies, Inc.
Registration dates
- Issuance Date
- November 18, 2019
- Expiry Date
- November 12, 2024
About this record
Access comprehensive regulatory information for VENOFIX® SAFETY WINGED IV NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01601 and manufactured by B. Braun Melsungen AG in Malaysia. The device was registered on November 18, 2019.
This page provides complete registration details including manufacturer information, importer/distributor details (B. Braun Medical Supplies, Inc.), 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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