FDA UDI In Commercial Distribution 🇺🇸 United States

microTargeting™ NexFrame® Insertion Tube Kit

DI: 00873263008485 · Model: 66-IT-4010S-00848 · FHC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
microTargeting™ NexFrame® Insertion Tube Kit
Primary DI
00873263008485
Version / Model
66-IT-4010S-00848
Catalog Number
66-IT-4010S
Company Name
FHC, INC.
Labeler DUNS
108179458
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-07
Public Version
1
Public Version Date
2021-12-15
Public Version Status
New
Public Device Record Key
f03178a0-49ca-45d6-8b8d-8e8c9a268893

Device Description

microTargeting Nexframe Insertion Tube Set with Stylet, Sterile. Contains: IT(KH3): Insertion Tube - 205.6mm tube length, 1.83mm od, 1.6mm id PT(KH1): Protective Tube - 0.58mm id. Nexframe Stylet.

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
62753 Intracerebral cannula, nonimplantable, single-use

Identifiers

Type ID
Package 10873263008482
Primary 00873263008485

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K011775 000

Storage Conditions

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