FDA UDI In Commercial Distribution 🇺🇸 United States

Navagio

DI: B073DRK0100330 · Model: DR-K01-0033 · Kalitec Direct LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Navagio
Primary DI
B073DRK0100330
Version / Model
DR-K01-0033
Catalog Number
DR-K01-0033
Company Name
Kalitec Direct LLC
Labeler DUNS
041956211
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-13
Public Version
1
Public Version Date
2023-09-21
Public Version Status
New
Public Device Record Key
e27f8cc9-17d6-4731-a9b8-bb7fc0a92373

Device Description

Assembly, Navagio Fixed Draw Rod, Large Knob

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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
32865 Orthopaedic implant driver

Identifiers

Type ID
Primary B073DRK0100330