FDA UDI In Commercial Distribution 🇺🇸 United States

microTargeting™ Insertion Tube

DI: 10873263007676 · Model: FC9002-00767 · FHC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
microTargeting™ Insertion Tube
Primary DI
10873263007676
Version / Model
FC9002-00767
Catalog Number
FC9002
Company Name
FHC, INC.
Labeler DUNS
108179458
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2019-12-31
Public Version
1
Public Version Date
2020-01-08
Public Version Status
New
Public Device Record Key
c543ffe3-6304-43a6-813c-784e58eb76fd

Device Description

microTargeting Array Lead Insertion Tube with Stylet, 5x, Sterile, for Nexframe and STarDrive

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
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
["Ethylene Oxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
62753 Intracerebral cannula, nonimplantable, single-use

Identifiers

Type ID
Primary 10873263007676
Unit of Use 00873263007679

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K092562 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 1.6 Millimeter
Length 218.35 Millimeter
Outer Diameter 1.83 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity
Type
Storage Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity