← Back to catalogue

Directional Laser Probe with Alcon / Lumenis connector.(20 gauge / 0.9 mm)

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
Directional Laser Probe with Alcon / Lumenis connector.(20 gauge / 0.9 mm) FDA UDI
Generic Name
Ophthalmic laser system beam guide FDA UDI
Model / Reference
7220.ALC FDA UDI

Identifiers

Primary DI / UDI-DI
08717872014142 FDA UDI
510(k) Number
K213467 FDA UDI
FDA Product Code
HQF FDA UDI
GMDN Term
Ophthalmic laser system beam guide FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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: Ophthalmic laser system beam guide

Directional Laser Probe with Alcon / Lumenis connector.(20 gauge / 0.9 mm) by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA…

Similar devices

Also classified as Ophthalmic laser system beam guide.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 62c6f090-1285-4d8b-9055-afc7e1bfaf84 33 fields · synced Jun 6, 2026