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EVA Nexus™ Infusion and Aux. Aspiration Tubing

FDA UDI

Class II (US FDA UDI)

by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Identity

Trade Name
EVA Nexus™ Infusion and Aux. Aspiration Tubing FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Model / Reference
9110.IAD02 FDA UDI

Identifiers

Primary DI / UDI-DI
08717872032962 FDA UDI
510(k) Number
K213467 FDA UDI
FDA Product Code
HQC FDA UDI
HQE FDA UDI
HQF FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 FDA UDI
886.4150 FDA UDI
886.4390 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation/aspiration tubing set

EVA Nexus™ Infusion and Aux. Aspiration Tubing by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd646aba-71da-4da0-a9f1-c33602cc8b67 33 fields · synced Jun 1, 2026