FDA UDI In Commercial Distribution 🇺🇸 United States

NeuLight®

DI: 00816901023372 · Model: WFS-365-RTSB · Weinert Fiber Optics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
NeuLight®
Primary DI
00816901023372
Version / Model
WFS-365-RTSB
Catalog Number
095612
Company Name
Weinert Fiber Optics, Inc.
Labeler DUNS
039281260
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-01
Public Version
2
Public Version Date
2023-05-02
Public Version Status
Update
Public Device Record Key
48cff22f-da55-4f0f-ac0c-afa7fac0bfb6

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
No
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 01816901023371
Primary 00816901023372
Package 02816901023370