MilliporeSigma

Entity profile compiled from public source records

Public Record Profile Registrations: 9 510(k) filings: 0 Recalls: 0

Known Identifiers & Locations

FEI Numbers 1000138378, 1000532580, 1937990, 1938173, 2244894, 3000718726, 3002638287, 3002807666, 3017212430
Owner Operator Numbers 1216103
Locations Covered Burlington, MA, US; COUNTY CORK Munster, IE; LIVINGSTON, W. LOTHIAN West Lothian, GB; MOLSHEIM Grand Est, FR; ROCKLIN, CA, US; ST. LOUIS, MO, US; Saint Louis, MO, US

Registered Establishments (9)

Registration # Establishment Name Location Establishment Type(s) Action
1000138378 SIGMA-ALDRICH CORP. Saint Louis, MO, US Complaint File Establishment per 21 CFR 820.198 View Details
1649339 CELL MARQUE CORP. ROCKLIN, CA, US Manufacture Medical Device for Another Party (Contract Manufacturer),Repack or Relabel Medical Device,Manufacture Medical Device View Details
1937990 SIGMA-ALDRICH MANUFACTURING, LLC-H&H Saint Louis, MO, US Manufacture Medical Device View Details
1938173 SIGMA-ALDRICH MANUFACTURING, LLC ST. LOUIS, MO, US Manufacture Medical Device for Another Party (Contract Manufacturer),Repack or Relabel Medical Device View Details
3009432145 EMD MILLIPORE CORPORATION Burlington, MA, US Complaint File Establishment per 21 CFR 820.198 View Details
3017212430 CELL MARQUE CORP. Saint Louis, MO, US Manufacture Medical Device,Repack or Relabel Medical Device View Details
8020892 Merck Millipore Ltd. COUNTY CORK Munster, IE Manufacture Medical Device View Details
9610805 MILLIPORE (UK) LTD LIVINGSTON, W. LOTHIAN West Lothian, GB Manufacture Medical Device View Details
9612003 MILLIPORE S.A.S MOLSHEIM Grand Est, FR Export Device to the United States But Perform No Other Operation on Device View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

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