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25ga Straight Laser Probe

FDA UDIEUDAMED

Class II (US FDA UDI)

by Vortex Surgical, Inc.

Identity

Trade Name
25ga Straight Laser Probe FDA UDI
Generic Name
Ophthalmic solid-state laser system FDA UDI
Device Name
25ga Straight Laser Probe FDA UDI
Model / Reference
VS0110.25 FDA UDI
Description
25ga Straight Laser Probe FDA UDI

Identifiers

Catalog Number
VS0110.25 FDA UDI
Primary DI / UDI-DI
VS01102517 FDA UDI
FDA Product Code
HQB FDA UDI
GMDN Term
Ophthalmic solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4690 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

Yes

FDA UDI

Category: Ophthalmic solid-state laser system

25ga Straight Laser Probe by Vortex Surgical, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic solid-state laser system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI fb1a8de3-5fc6-4828-8767-e9a52d0998ec 35 fields · synced Jun 17, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026