FDA UDI In Commercial Distribution 🇺🇸 United States

InvisiShunt Cutting Guide

DI: 00855113008432 · Model: OP5002 · LONGEVITI NEURO SOLUTIONS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
InvisiShunt Cutting Guide
Primary DI
00855113008432
Version / Model
OP5002
Company Name
LONGEVITI NEURO SOLUTIONS LLC
Labeler DUNS
070659539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-27
Public Version
1
Public Version Date
2023-04-04
Public Version Status
New
Public Device Record Key
2ea87044-df90-476b-bf97-7ba38317ba10

Device Description

InvisiShunt Cutting Guide (OP5002)

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

GMDN Terms

Code Name
33310 Polyethylene craniofacial tissue reconstructive material

Identifiers

Type ID
Primary 00855113008432

Premarket Submissions

Submission Number Supplement Number
K211514 000