FDA UDI In Commercial Distribution 🇺🇸 United States

KIT PATIENT

DI: 03770022347229 · Model: KIT · MODJAW
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KIT PATIENT
Primary DI
03770022347229
Version / Model
KIT
Catalog Number
KIT
Company Name
MODJAW
Labeler DUNS
265572589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-23
Public Version
1
Public Version Date
2022-03-03
Public Version Status
New
Public Device Record Key
a37f59b2-086d-4160-a0e6-1e2bf7639390

Device Description

A set of trackers intended to be placed on the patient’s head and in patient’s mouth including : - Mandibular tracker - Frontal tracker - pen tracker

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NFS Device, Jaw Tracking, For Monitoring Jaw Positions

GMDN Terms

Code Name
47556 Jaw physiology evaluation system

Identifiers

Type ID
Primary 03770022347229

Customer Contacts

Phone
+33482771111