← Back to catalogue

EVA NEXUS™ Combined 27G TDC Pack

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 9310.27G02

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

Identity

Trade Name
EVA NEXUS Combined 27G TDC Pack EUDAMED
EVA NEXUS™ Combined 27G TDC Pack FDA UDI
Generic Name
Ophthalmic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
EVA NEXUS Combined 27G TDC Pack EUDAMED
Model / Reference
9310.27G02 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08717872032917 EUDAMEDFDA UDI
Basic UDI-DI
B-08717872032917 EUDAMED
510(k) Number
K213467 FDA UDI
FDA Product Code
HQC FDA UDI
HQE FDA UDI
EMDN Code
Z1212020785 PHACO-VITRECTOMY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
886.4670 FDA UDI
886.4150 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Ophthalmic surgical procedure kit, non-medicated, single-use

EVA NEXUS™ Combined 27G TDC Pack by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 84b35853-845c-4c70-aa6f-a78de2bc302a 33 fields · synced Oct 8, 2026
  • EUDAMED 7ea9ffaa-a270-46bd-934a-14e2fe0e867a 61 fields · synced Oct 8, 2026