This page includes the latest FDA filings for Simpleware Product Group Synopsys Northern Europe. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3011676026 | ||||||
| FEI Number | 3011676026 | ||||||
| Name | Simpleware Product Group, SYNOPSYS NORTHERN EUROPE | ||||||
| Owner & Operator | Synopsys Northern Europe | ||||||
| Contact Address | Bradninch Hall, Castle Street Exeter GB-DEV Devon EX4 3PL GB | ||||||
| Official Correspondent |
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| US Agent |
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| Importing Logistics Registration |
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| Registration Status | 1 | ||||||
| Initial Importer | N | ||||||
| Registration Expiration | 2020-04-25 | ||||||
| Registration Address | Bradninch Hall, Castle Street Exeter Devon, EX4 3PL GB | ||||||
| Establishment Type | Complaint File Establishment per 21 CFR 820.198 |
Device Company | Device | Date |
|---|---|---|
Simpleware Product Group, SYNOPSYS NORTHERN EUROPE [Synopsys Northern Europe] | Simpleware ScanIP Medical | 2015-04-24 |