FDA UDI Not in Commercial Distribution 🇺🇸 United States

NeuLight®

DI: 00816901023310 · Model: WFS-600-SB · Weinert Fiber Optics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NeuLight®
Primary DI
00816901023310
Version / Model
WFS-600-SB
Catalog Number
095632
Company Name
Weinert Fiber Optics, Inc.
Labeler DUNS
039281260
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-12
Public Version
1
Public Version Date
2026-03-20
Public Version Status
New
Public Device Record Key
7682ad23-6895-4f3e-94b0-b7c485a2c330
Distribution End Date
2026-03-12

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
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
GEX Powered laser surgical instrument

GMDN Terms

Code Name
47785 Urogenital surgical laser system beam guide, single-use

Identifiers

Type ID
Package 02816901023318
Package 01816901023319
Primary 00816901023310