This page includes the latest FDA filings for Axlab Innovation A P S. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3003192451 |
| FEI Number | 3003192451 |
| Name | Biopsafe APS |
| Owner & Operator | Axlab Innovation Aps |
| Contact Address | Bygstubben 4 Vedbaek DK-84 Region Hovedstaden 2950 DK |
| Official Correspondent |
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| US Agent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | Bygstubben 4 Vedbaek Region Hovedstaden, 2950 DK |
| Establishment Type | Develop Specifications But Do Not Manufacture At This Facility |
Device Company | Device | Date |
|---|---|---|
Biopsafe APS [Axlab Innovation Aps] | BiopSafe | 2016-02-03 |
| Import ID | Shipment | Cargo Description | Quantity |
|---|---|---|---|
| 2018061247541 | Bremerhaven,Federal Republic of Germany -> Norfolk, Virginia | MEDICAL SUPPLIES HS: 291211 | 2 PKG |
| 201804207524 | Stadersand,Federal Republic of Germany -> Oakland, California | MEDICAL EQUIPMENT LOADED ONTO 4 PALLETS HS-CODE 291211 | 144 PKG |