Philippines FDA registration MDR-09929
TWINFIX ULTRA HA WITH NEEDLE
Philippines·Smith & Nephew Endoscopy·USA·Issued July 08, 2020 – July 08, 2021Device information
- Product Name
- TWINFIX ULTRA HA WITH NEEDLE
- Registration Number
- MDR-09929
Manufacturer details
- Manufacturer
- Smith & Nephew Endoscopy
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Endomed Trading, Inc.
Registration dates
- Issuance Date
- July 08, 2020
- Expiry Date
- July 08, 2021
About this record
Access comprehensive regulatory information for TWINFIX ULTRA HA WITH NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09929 and manufactured by Smith & Nephew Endoscopy in USA. The device was registered on July 08, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (Endomed Trading, 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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