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926823G Two Dimensional Cutter – 20k CPM

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
926823G Two Dimensional Cutter – 20k CPM FDA UDI
Generic Name
Ophthalmic surgical instrument handle, pneumatic FDA UDI
Model / Reference
9268.VIT23-00 FDA UDI

Identifiers

Catalog Number
9268.VIT23-00 FDA UDI
Primary DI / UDI-DI
08717872036519 FDA UDI
510(k) Number
K213467 FDA UDI
FDA Product Code
HQE FDA UDI
GMDN Term
Ophthalmic surgical instrument handle, pneumatic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4150 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: Ophthalmic surgical instrument handle, pneumatic

926823G Two Dimensional Cutter – 20k CPM 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 Ophthalmic surgical instrument handle, pneumatic.

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 31ea8cb8-4b30-47b1-b8da-da56486d7826 34 fields · synced Jun 8, 2026