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HEALICOIL® SA PK SUTURE ANCHOR WITH THREE ULTRABRAID (#2) SUTURES - FDA Registration MDR-04800C

Access comprehensive regulatory information for HEALICOIL® SA PK SUTURE ANCHOR WITH THREE ULTRABRAID (#2) SUTURES in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04800C and manufactured by Smith & Nephew Private Limited in USA. The device was registered on November 26, 2018.

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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MDR-04800C
HEALICOIL® SA PK SUTURE ANCHOR WITH THREE ULTRABRAID (#2) SUTURES
Registered medical device in Philippines
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Device Information
Product Name
HEALICOIL® SA PK SUTURE ANCHOR WITH THREE ULTRABRAID (#2) SUTURES
Registration Number
MDR-04800C
Manufacturer Details
Country of Origin
USA
Importer & Distribution
Importer/Distributor
Endomed Trading Inc.
Registration Dates
Issuance Date
November 26, 2018
Expiry Date
August 10, 2023