# Sartorius Stedim Lab Ltd.

FEI: 3007699074
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Owner/operator: Sartorius Stedim North America Inc./Sartorius Corporation (#9005426)

Address: Sperry Way, Stonehouse Park, Stonehouse Gloucestershire, GL10 3UT, GB

Mandatory US Agent: Sartorius Stedim North America Inc.

## Products

Total registered: 1
Top product codes: JJH
Regulation §: 862.2310

Proprietary names: Vivaspin 6 (VS0601IVD, VS0602IVD), Vivaspin 15 Turbo (VS15T01IVD, VS15T02IVD), Vivaspin 4 Turbo (VS04T01IVD, VS04T02IVD), Vivafree 500 30K (VFR01H21,VFR01H22,VFR01H23), Vivafree 500 125K (VFR01H81,VFR01H82,VFR01H83), Vivaspin 20 (VS2001IVD, VS2002IVD), Centrisart 100k (13269----------E), Vivafree 2 125K (VFR02H81,VFR02H82,VFR02H83), Vivapore 5 (VP0503, VP0501), Vivaspin 4 10K (VS0404, VS0405)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007699074%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007699074