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PORTEX COMBINED SPINA/EPIDURAL MINIPACK WITH LOCK PENCIL POINT SPINAL NEEDLE - FDA Registration MDR-04845

Access comprehensive regulatory information for PORTEX COMBINED SPINA/EPIDURAL MINIPACK WITH LOCK PENCIL POINT SPINAL NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04845 and manufactured by Smiths Medical ASD, Inc. in USA. The device was registered on August 15, 2017.

This page provides complete registration details including manufacturer information, importer/distributor details (Rebmann, 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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USA
MDR-04845
PORTEX COMBINED SPINA/EPIDURAL MINIPACK WITH LOCK PENCIL POINT SPINAL NEEDLE
Registered medical device in Philippines
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Device Information
Product Name
PORTEX COMBINED SPINA/EPIDURAL MINIPACK WITH LOCK PENCIL POINT SPINAL NEEDLE
Registration Number
MDR-04845
Manufacturer Details
Country of Origin
USA
Importer & Distribution
Importer/Distributor
Rebmann, Inc.
Registration Dates
Issuance Date
August 15, 2017
Expiry Date
October 19, 2022