Philippines FDA registration MDR-08796I
BMAC2-120n BONE MARROW PROCEDURE PACK
Philippines·Terumo BCT, Inc. - Lakewood, CO, USA·USA·Issued June 11, 2021 – October 17, 2025Device information
- Product Name
- BMAC2-120n BONE MARROW PROCEDURE PACK
- Registration Number
- MDR-08796I
Manufacturer details
- Manufacturer
- Terumo BCT, Inc. - Lakewood, CO, USA
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Terumo Markerting Philippines, Inc.
Registration dates
- Issuance Date
- June 11, 2021
- Expiry Date
- October 17, 2025
About this record
Access comprehensive regulatory information for BMAC2-120n BONE MARROW PROCEDURE PACK in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08796I and manufactured by Terumo BCT, Inc. - Lakewood, CO, USA in USA. The device was registered on June 11, 2021.
This page provides complete registration details including manufacturer information, importer/distributor details (Terumo Markerting Philippines, 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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