FDA UDI In Commercial Distribution 🇺🇸 United States

Nextra Hammertoe Correction System

DI: 00817701020837 · Model: NX-DR · Medartis Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Nextra Hammertoe Correction System
Primary DI
00817701020837
Version / Model
NX-DR
Company Name
Medartis Inc.
Labeler DUNS
192756786
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-12
Public Version
8
Public Version Date
2023-09-29
Public Version Status
Update
Public Device Record Key
6554218b-676a-41e0-ab2c-a44ca8a6d434

Device Description

Nextra Driver

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
Yes
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
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
58776 Surgical screwdriver, single-use

Identifiers

Type ID
Primary 00817701020837