Philippines FDA registration MDR-09906
SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR
Philippines·Smith & Nephew Pte. Ltd.·USA·Issued July 02, 2020 – July 02, 2021Device information
- Product Name
- SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR
- Registration Number
- MDR-09906
Manufacturer details
- Manufacturer
- Smith & Nephew Pte. Ltd.
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Endomed Trading, Inc.
Registration dates
- Issuance Date
- July 02, 2020
- Expiry Date
- July 02, 2021
About this record
Access comprehensive regulatory information for SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09906 and manufactured by Smith & Nephew Pte. Ltd. in USA. The device was registered on July 02, 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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