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Sign in to claim this brandTerumo 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
- —
- Website
- terumomedical.com
- —
- —
- [email protected]
- Phone
- +1(800)283-7866
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 370193559
Catalogue (66)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Syringe with fixed needle - For use only with GONAL-f Multi-Dose 600 IU/mL FSH | BS-N1A2713U10 | FDA UDI | Class II | Unknown |
| K-Pack Embrace™ | KNAS-2525RB | FDA UDI | Class II | Active |
| K-Pack II | KN-1838SBS | FDA UDI | Class II | Active |
| K-Pack II | KN-2713RB500P | FDA UDI | Class II | Active |
| K-Pack II Needle | KN-2719RBT500P | FDA UDI | Class II | Active |
| K-Pack II | KN-3013RKT50 | FDA UDI | Class II | Active |
| K-Pack II | KN-2719RB500P | FDA UDI | Class II | Active |
| K-Pack II | KN-1938RB | FDA UDI | Class II | Active |
| K-Pack II | KN-3013RBKT | FDA UDI | Class II | Active |
| K-Pack II | KN-2913RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2719RB | FDA UDI | Class II | Active |
| K-Pack Surshield™ | KN-S2713RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2713RBR | FDA UDI | Class II | Active |
| Terumo | NF-3013RBKE05M | FDA UDI | Class II | Active |
| K-Pack II | KN-2719RBTS | FDA UDI | Class II | Active |
| K-Pack II | KN-2713RBKT | FDA UDI | Class II | Active |
| K-Pack II | KN-2525RB | FDA UDI | Class II | Active |
| K-Pack II | KN-3013RBKE | FDA UDI | Class II | Active |
| K-Pack Surshield™ | KN-S2516RB | FDA UDI | Class II | Active |
| Surguard™3 | SG3-1938RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2616RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2913RBKT | FDA UDI | Class II | Active |
| K-Pack II | KN-2525RB04 | FDA UDI | Class II | Active |
| K-Pack II | KN-2713RBKT50 | FDA UDI | Class II | Unknown |
| K-Pack II | KN-2913RBS | FDA UDI | Class II | Active |
| Terumo | KH-2913RBBTC | FDA UDI | Class II | Active |
| K-Pack II | KN-2232RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2610RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2138RB04 | FDA UDI | Class II | Active |
| Surguard™3 | SG3-2516RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2325RB04 | FDA UDI | Class II | Active |
| K-Pack II | KN-2516RB05 | FDA UDI | Class II | Active |
| K-Pack II | KN-2908RBKT | FDA UDI | Class II | Active |
| K-Pack II | KN-3013RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2713RKT50 | FDA UDI | Class II | Active |
| Surflo™ | SV-S23BL35 | FDA UDI | Class II | Active |
| K-Pack Embrace™ | KNAS-2516RB | FDA UDI | Class II | Active |
| Surflo™ | SV-S25BL35 | FDA UDI | Class II | Active |
| K-Pack II | KN-2325RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2516RB04 | FDA UDI | Class II | Active |
| K-Pack II | KN-2038RB500P | FDA UDI | Class II | Active |
| K-Pack II | KN-2238RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2713RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2713RBKTU | FDA UDI | Class II | Active |
| K-Pack II | KN-2138RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2150RB | FDA UDI | Class II | Active |
| K-Pack II | KN-2719RBT | FDA UDI | Class II | Active |
| Surflo™ | SV-S25WL35 | FDA UDI | Class II | Active |
| Syringe with fixed needle - For use only with GONAL-f Multi-Dose 600IU/ml FSH | BS-N1A2713U | FDA UDI | Class II | Active |
| K-Pack II | KN-2713RBK | FDA UDI | Class II | Active |
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