ARJOHUNTLEIGH AB

Entity profile compiled from public source records

Public Record Profile Registrations: 8 510(k) filings: 0 Recalls: 0

Known Identifiers & Locations

FEI Numbers 1000589001, 3002655016, 3002806395, 3005619970, 3007420694, 3007518069, 3010010434, 3012292104
Owner Operator Numbers 10028687, 10036598, 10051620, 8010077, 9026070
Locations Covered CARDIFF, SOUTH GLAMORGAN, GB; Eindhoven Noord-Brabant, NL; Itabo, Haina San Cristobal, DO; MAGOG Quebec, CA; MALMO Skane, SE; Mississauga Ontario, CA; Poznan Wielkopolskie, PL; Suzhou Jiangsu, CN

Registered Establishments (8)

Registration # Establishment Name Location Establishment Type(s) Action
1000589001 HUNTLEIGH HEALTHCARE LTD. CARDIFF, SOUTH GLAMORGAN, GB Manufacture Medical Device View Details
3002806395 ARJOHUNTLEIGH AB MALMO Skane, SE Develop Specifications But Do Not Manufacture At This Facility View Details
3005619970 Arjo (Suzhou) Co., Ltd. Suzhou Jiangsu, CN Manufacture Medical Device for Another Party (Contract Manufacturer) View Details
3007420694 ArjoHuntleigh Polska Sp. zo.o. Poznan Wielkopolskie, PL Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility View Details
3007518069 ARJOHUNTLEIGH LOGISTICS Eindhoven Noord-Brabant, NL Export Device to the United States But Perform No Other Operation on Device View Details
3010010434 Arjo Canada Inc. Mississauga Ontario, CA Export Device to the United States But Perform No Other Operation on Device View Details
3012292104 Arjo Dominican Republic Itabo, Haina San Cristobal, DO Manufacture Medical Device View Details
9681684 ARJOHUNTLEIGH MAGOG, INC. MAGOG Quebec, CA Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility 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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