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TotalView Endoillumination Probe, with 2 exchangeable tips.(23 gauge / 0.6 mm)

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 3269.E06

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

Identity

Trade Name
TotalView Endoillumination Probe, with 2 exchangeable tips (23 gauge / 0.6 mm) EUDAMED
TotalView Endoillumination Probe, with 2 exchangeable tips.(23 gauge / 0.6 mm) FDA UDI
Generic Name
Ophthalmic fibreoptic light instrument, single-use FDA UDI
Device Name
TotalView Endoillumination Probe, with 2 exchangeable tips (23 gauge / 0.6 mm) EUDAMED
Model / Reference
3269.E06 EUDAMEDFDA UDI

Identifiers

Catalog Number
3269.E06 FDA UDI
Primary DI / UDI-DI
08717872009452 EUDAMEDFDA UDI
Basic UDI-DI
B-08717872009452 EUDAMED
510(k) Number
K062895 FDA UDI
FDA Product Code
MPA FDA UDI
EMDN Code
Z12129085 VARIOUS OPHTALMOLOGY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Ophthalmic fibreoptic light instrument, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1500 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 fibreoptic light instrument, single-use

TotalView Endoillumination Probe, with 2 exchangeable tips.(23 gauge / 0.6 mm) by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II…

Similar devices

Also classified as Ophthalmic fibreoptic light instrument, single-use.

Cleared under the same submission

K062895 also covers:

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI b969da4d-98a4-4329-b02e-6ab4a92c2963 34 fields · synced Oct 8, 2026
  • EUDAMED ef5e8df3-ad8b-4db0-aba5-6428ed68d3c4 61 fields · synced Oct 7, 2026