DEVICE: microTargeting™ Lead Insertion Tube with Stylet (00873263006498)
Device Identifier (DI) Information
microTargeting™ Lead Insertion Tube with Stylet
66-IT-AR14P-00649
In Commercial Distribution
66-IT-AR14P
FHC, INC.
66-IT-AR14P-00649
In Commercial Distribution
66-IT-AR14P
FHC, INC.
microTargeting™ Lead Insertion Tube with Stylet, Sterile, for use with stereotactic frame, 5x
Device Characteristics
| MR Unsafe | |
| No | |
| No | |
| Yes | |
| Yes | |
| No | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 62753 | Intracerebral cannula, nonimplantable, single-use |
A sterile, nonimplantable, rigid tube intended to be surgically inserted through the skull to access the brain (e.g., cerebral ventricles) for cerebrospinal fluid (CSF) drainage, infusion of materials, and/or for use as a port through which instruments, leads and/or probes can be passed to perform a variety of diagnostic, treatment, or surgical procedures. It is usually made of metal (e.g., stainless steel) and may include a stylet/trocar blade. This is a single-use device.
|
Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| HAW | Neurological stereotaxic Instrument |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| K011775 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Storage Environment Temperature: between 0 and 40 Degrees Celsius |
| Handling Environment Humidity: between 0 and 95 Percent (%) Relative Humidity |
| Storage Environment Humidity: between 0 and 95 Percent (%) Relative Humidity |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Lumen/Inner Diameter: 1.6 Millimeter |
| Outer Diameter: 1.83 Millimeter |
| Length: 267.85 Millimeter |
Device Record Status
c4136f5a-5b19-4134-83ac-b8458e6cd9e0
July 06, 2018
3
February 05, 2018
July 06, 2018
3
February 05, 2018
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| 10873263006495 | 5 | 00873263006498 | In Commercial Distribution | PK/5 |
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)326-2905
fhcinc@fh-co.com
fhcinc@fh-co.com