FDA Registration
Active
🇸🇪 Sweden
CELLAVISION AB
Reg #: 3003630693
·
FEI: 3003630693
·
Expires 2026
Products
4
Proprietary Names
14
Establishment Types
5
Classifications
4
Registration Details
- Registration Name
- CELLAVISION AB
- Registration Number
- 3003630693
- FEI Number
- 3003630693
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- Mobilvagen 12
- City
- LUND Skane
- Country
- SE
Regulatory Submissions
- 510(k) Number
- K102778
Owner / Operator
- Firm Name
- CellaVision AB
- Operator Number
- 9043433
- Address
- Mobilvagen 12, --
- City
- LUND
- State
- SE-NOTA
- Postal Code
- SE-22362
- Country
- SE
- Correspondent
- Charlotte - Oom
US Agent
- Business Name
- -
- Contact Name
- Scott Dunbar
- Address
- 2530 Meridian Pkwy, Suite 300, -
- City
- Durham
- State
- NC
- ZIP
- 27713
- Country
- US
- [email protected]
- Phone
- 919 8064420
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Device, Automated Cell-Locating | JOY | Class 2 | Hematology | No | 2011-11-03 |
| Counter, Differential Cell | GKZ | Class 2 | Hematology | No | 2010-07-07 |
| Medical Device Data System | OUG | Class 1 | General Hospital | No | 2017-06-19 |
| Spinner, Slide, Automated | GKJ | Class 1 | Hematology | No | 2018-08-30 |
Proprietary Names
CellaVision Body Fluid Application for DM1200, DM9600 and DI-60
CellaVision Body Fluid Application
Cellavision Body Fluid Application Non-Expiring license, DM96
CellaVision Server Software
CellaVision DM96 and DM1200 with Advanced RBC Application
DI-60 with Advanced RBC Application
CellaVision DM9600 with Advanced RBC Application
HemaPrep
Automated Digital Cell Morphology Analyzer DI-60
CellaVision DM9600
CellaVision DM1200
CellaVision DC-1
CellaVision DC-1 PPA
CellaVision DM96
Establishment Types
Develop Specifications But Do Not Manufacture At This Facility
Export Device to the United States But Perform No Other Operation on Device
Manufacture Medical Device
Complaint File Establishment per 21 CFR 820.198
Repack or Relabel Medical Device