FDA UDI In Commercial Distribution 🇺🇸 United States

Vertex

DI: 00810005663939 · Model: STK-1000C-003 · NVISION BIOMEDICAL TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vertex
Primary DI
00810005663939
Version / Model
STK-1000C-003
Company Name
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Labeler DUNS
047486041
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-05
Public Version
1
Public Version Date
2021-05-13
Public Version Status
New
Public Device Record Key
37cf5015-4b59-4db6-ac03-f03587e6f7c7

Device Description

Vertex Reusable Tray Caddy Base. The Vertex Nitinol Staple System consists of a series of nickel titanium alloy staple implants and the instruments necessary for the treatment of pathologies of the foot and ankle. The Vertex bone staples are made from superelastic nitinol that does not require cold storage or heating.

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LRP Tray, Surgical

GMDN Terms

Code Name
42997 Surgical instrument/implant rack

Identifiers

Type ID
Primary 00810005663939

Customer Contacts