← Back to catalogue

23ga Flexible Tapered Illuminated Laser Probe, Alcon Compatible

FDA UDI

Class II (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
23ga Flexible Tapered Illuminated Laser Probe, Alcon Compatible FDA UDI
Generic Name
Ophthalmic fibreoptic light instrument, single-use FDA UDI
Device Name
23ga Flexible Tapered Illuminated Laser Probe, Alcon Compatible FDA UDI
Model / Reference
V6315-23BR FDA UDI
Description
23ga Flexible Tapered Illuminated Laser Probe, Alcon Compatible FDA UDI

Identifiers

Primary DI / UDI-DI
10817489023775 FDA UDI
510(k) Number
K121187 FDA UDI
FDA Product Code
HQF FDA UDI
GMDN Term
Ophthalmic fibreoptic light instrument, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4390 FDA UDI
Commercial Distribution
Not 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

No

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

23ga Flexible Tapered Illuminated Laser Probe, Alcon Compatible by Katalyst Surgical, Llc — Class II — FDA UDI — listed in FDA GUDID

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 f56c5612-63c1-42dd-b219-c69829b4aa35 35 fields · synced May 30, 2026