FDA UDI In Commercial Distribution 🇺🇸 United States

NEXDRIVE™ w/DIG

DI: 00873263008706 · Model: MI-1000-00870 · FHC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NEXDRIVE™ w/DIG
Primary DI
00873263008706
Version / Model
MI-1000-00870
Catalog Number
MI-1000
Company Name
FHC, INC.
Labeler DUNS
108179458
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-30
Public Version
1
Public Version Date
2025-05-08
Public Version Status
New
Public Device Record Key
fb2cd41d-d26b-4316-9ca4-7a9c490a3da4

Device Description

MI-1000 NEXDRIVE™ Micropositioning Drive with Display Option

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
Yes
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 00873263008706

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K022100 000

Storage Conditions

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