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MEDIPURPOSE PTE. LTD.

US

Last updated May 24, 2026

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
(404) 855-3655
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
628380248

Catalogue (55)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Babylance Heel Incision Device , Models Blp50, Blp200, Bln50, Bln200 K101417
FDA 510(k)
Class IIActive
Surgilance Safety Lancets, Models Sln100, Sln200, Sln240, Sln300, Slb200, Slb250 K101145
FDA 510(k)
Class IIActive
Mediplus-Foam Ag; Mediplus-Comfortfoam Ag; Mediplus-Superfoam Ag K110062
FDA 510(k)
UActive
SurgiLance® Safety Lancet K222224
FDA 510(k)
Class IIActive
Babylance Heel Incision Device K130132
FDA 510(k)
Class IIActive

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Medipurpose Pte. Ltd. SINGAPORE Central Singapore · SG FEI 3008179438