FDA UDI In Commercial Distribution 🇺🇸 United States

Fiber Optic Light Cable

DI: 00857580006744 · Model: 4.6mm bundle diameter, 9.9' length, Bifurcated Cable · GULF FIBEROPTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Fiber Optic Light Cable
Primary DI
00857580006744
Version / Model
4.6mm bundle diameter, 9.9' length, Bifurcated Cable
Catalog Number
169-500-S
Company Name
GULF FIBEROPTICS, INC.
Labeler DUNS
017416582
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-04
Public Version
1
Public Version Date
2020-05-12
Public Version Status
New
Public Device Record Key
02f39994-3258-4667-985b-fbe6b0972aa0

Device Description

A sterile device with a fibreoptic bundle core designed to be affixed to the surface of a surgical instrument, typically a retractor, to conduct cold light from a connected fibreoptic light cable and light source into a surgical wound for illumination during a surgical intervention. It typcially emits cold light only through its tip to eliminate glare, and may have a self-adhesive coating for attachment to the surgical instrument. This is a single-use device.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FDG Retractor, Fiberoptic

GMDN Terms

Code Name
48036 Surgical instrument fibreoptic light

Identifiers

Type ID
Primary 00857580006744

Customer Contacts

Phone
815-855-6618