AccessGUDID - DEVICE: 20ga Straight Illuminated Laser Probe, 19ga Needle Illumination, Alcon (10817489023577)

GUDID

Device Identifier (DI) Information

Brand Name: 20ga Straight Illuminated Laser Probe, 19ga Needle Illumination, Alcon
Version or Model: V6300-20BR
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: KATALYST SURGICAL LLC

Primary DI Number: 10817489023577
Issuing Agency: GS1
Commercial Distribution End Date: July 01, 2025
Device Count: 10
Labeler D-U-N-S® Number*: 007883297 *Terms of Use

Device Description: 20ga Straight Illuminated Laser Probe, 19ga Needle Illumination, Alcon

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
45193	Ophthalmic fibreoptic light instrument, single-use	A sterile, hand-held, ophthalmic surgical instrument with a thin, rigid, insertion portion, that is inserted into the eye during a surgical intervention for the purpose of conducting a field of cold light to the posterior segment of the eye. It is connected through a permanently attached light cable to a light source. It has a fibreoptic bundle core that conducts the light, and may be provided with an atraumatic tip to allow for extraocular manipulation (orbital depression) with transscleral illumination. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HQF	Laser, Ophthalmic

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K121187	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: cf2aef4d-81ec-443a-a5f4-bba97137eef3
Public Version Date: July 03, 2025
Public Version Number: 2
DI Record Publish Date: November 27, 2020