Skip to content

Applied Medical Europe

Also registered as Applied Medical Europe B.V.

Netherlandsfrom SRN FDA establishment FEI 3009763019

Devices
462
Registrations
FDA
FDA recalls
0

Catalogue462

Newest first, rows 301-350 of 462

Search and filter all 462 devices
Skip device list

  • Ame Standard Kit Ref CK089

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CL105

    Class IIb
    Active CE MDR EUDAMED IIb

  • GK1000

    Class IIb
    Active CE MDR EUDAMED IIb

  • Ame Standard Kit Ref CK208

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref GK809

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK047

    Class IIa
    Active CE MDR EUDAMED IIa

  • GK1095

    Class IIa
    Active CE MDR EUDAMED IIa

  • CK274

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK223

    Class IIa
    Active CE MDR EUDAMED IIa

  • GK1057

    Class IIb
    Active CE MDR EUDAMED IIb

  • Ame Standard Kit Ref CK239

    Class IIb
    Active CE MDR EUDAMED IIb

  • GK1050

    Class IIa
    Active CE MDR EUDAMED IIa

  • GK1096

    Class IIb
    Active CE MDR EUDAMED IIb

  • CK591

    Class IIa
    Active CE MDR EUDAMED IIa

  • CK283

    Class IIa
    Active CE MDR EUDAMED IIa

  • GK1009

    Class IIb
    Active CE MDR EUDAMED IIb

  • Ame Standard Kit Ref CK006

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK010

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK241

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK060

    Class IIa
    Active CE MDR EUDAMED IIa

  • CK569

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK243

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK242

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK094

    Class IIa
    Active CE MDR EUDAMED IIa

  • GK225

    Class IIa
    Active CE MDR EUDAMED IIa

  • CK284

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK1011

    Class IIa
    Active CE MDR EUDAMED IIa

  • GK1090

    Class IIa
    Active CE MDR EUDAMED IIa

  • CK593

    Class IIa
    Active CE MDR EUDAMED IIa

  • GK247

    Class IIa
    Active CE MDR EUDAMED IIa

  • GK1085

    Class IIb
    Active CE MDR EUDAMED IIb

  • Ame Standard Kit Ref CK040

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK240

    Class IIb
    Active CE MDR EUDAMED IIb

  • CK573

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref GK812

    Class IIb
    Active CE MDR EUDAMED IIb

  • Ame Standard Kit Ref CK228

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK202

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK1003

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK090

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK1045

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref GK792

    Class IIa
    Active CE MDR EUDAMED IIa

  • CK273

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref GK1051

    Class IIa
    Active CE MDR EUDAMED IIa

  • CK547

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK249

    Class IIa
    Active CE MDR EUDAMED IIa

  • CK268

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK258

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK1008

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK234

    Class IIa
    Active CE MDR EUDAMED IIa

  • Ame Standard Kit Ref CK1014

    Class IIa
    Active CE MDR EUDAMED IIa

Rows 301-350 of 462

Showing 301-350 of 462

Company details

FDA FEI number
3009763019
Address
Wiekenweg 21, Amersfoort Utrecht

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.