FDA UDI In Commercial Distribution 🇺🇸 United States

UltraLase Flexible Laser Waveguide

DI: 00866988000209 · Model: HWG500-2.0-3.0 · LASER ENGINEERING
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
UltraLase Flexible Laser Waveguide
Primary DI
00866988000209
Version / Model
HWG500-2.0-3.0
Catalog Number
HWG500-2.0-3.0
Company Name
LASER ENGINEERING
Labeler DUNS
028541358
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
4
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
642ab44b-230d-482c-824c-16e1eecc41bd

Device Description

This device is an internally coated fused silica waveguide used to deliver CO2 laser energy to the patient

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
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
Primary 00866988000209
Package 10866988000206

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K112166 000