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Terumo Europe NV

US

Last updated May 27, 2026

What Terumo Europe NV makes

The company manufactures single-use hypodermic needles and basic intravenous administration sets designed for medical procedures. Their portfolio includes metered-delivery hypodermic syringes and ophthalmic needles, primarily used in injections, fluid administration, and specialized surgical applications.

These devices are classified as Class II under regulatory standards, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable regulatory requirements for medical devices.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+1(800)283-7866
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
370193559

Catalogue (66)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
K-Pack II KN-2038RB
FDA UDI
Class IIActive
K-Pack II KN-2232RBB
FDA UDI
Class IIActive
K-Pack II KN-2713RBKTE
FDA UDI
Class IIActive
Syringe with fixed needle - For use only with GONAL-f Multi-Dose 600 IU/mL FSH BS-N1A2713U6
FDA UDI
Class IIUnknown
Surguard™3 SG3-1925RB
FDA UDI
Class IIActive
K-Pack Surshield™ KN-S2713RBT
FDA UDI
Class IIActive
Terumo KH-2713RBBTC
FDA UDI
Class IIActive
K-Pack II KN-1838SB
FDA UDI
Class IIActive
Surflo™ SV-S25WL35C
FDA UDI
Class IIActive
K-Pack II KN-2332RB
FDA UDI
Class IIActive
Surflo™ SV-S23FL35
FDA UDI
Class IIActive
Surflo™ SV-S23WL35
FDA UDI
Class IIActive
K-Pack II KN-3013RBKU
FDA UDI
Class IIActive
Surguard™3 SG3-2138RB
FDA UDI
Class IIActive
Surflo™ SV-S25FL35C
FDA UDI
Class IIActive
Surflo™ SV-S25FL35
FDA UDI
Class IIActive

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