FDA UDI In Commercial Distribution 🇺🇸 United States

Twister

DI: 00859337007035 · Model: 101175-IC · WISDOM MEDICAL TECHNOLOGY, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Twister
Primary DI
00859337007035
Version / Model
101175-IC
Catalog Number
101175-IC
Company Name
WISDOM MEDICAL TECHNOLOGY, LLC
Labeler DUNS
080537625
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-02
Public Version
6
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
0853f8b9-4bca-4186-84e5-0dae4266f430

Device Description

lateral emitting laser fiber

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
61474 General/multiple surgical laser system beam guide, reusable

Identifiers

Type ID
Primary 00859337007035

Customer Contacts

Phone
630-803-6383

Premarket Submissions

Submission Number Supplement Number
K112987 000