This page includes the latest FDA filings for 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 |