FDA UDI In Commercial Distribution 🇺🇸 United States

NEXDRIVE™

DI: 00873263007723 · Model: MI-2000-00772 · FHC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NEXDRIVE™
Primary DI
00873263007723
Version / Model
MI-2000-00772
Catalog Number
MI-2000
Company Name
FHC, INC.
Labeler DUNS
108179458
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-02
Public Version
1
Public Version Date
2020-11-10
Public Version Status
New
Public Device Record Key
f990fe02-b932-442d-8de8-0a3f164e339c

Device Description

MI-2000 NEXDRIVE™ Micropositioning Drive

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

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
32568 Neurological stereotactic surgery system

Identifiers

Type ID
Primary 00873263007723

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K022100 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-34 – 57 Degrees Celsius