FDA UDI In Commercial Distribution 🇺🇸 United States

Guideline 4000™ 5.0

DI: 00873263006795 · Model: C0217-00679 · FHC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Guideline 4000™ 5.0
Primary DI
00873263006795
Version / Model
C0217-00679
Catalog Number
C0217
Company Name
FHC, INC.
Labeler DUNS
108179458
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-02
Public Version
2
Public Version Date
2020-02-19
Public Version Status
Update
Public Device Record Key
7d0566fd-0cb9-4c6b-aff1-a14a5df97d99

Device Description

MicroTargeting Guidline 4000 5.0 Software 1x

Device Characteristics

Single Use
No
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
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GZL ELECTRODE, DEPTH

GMDN Terms

Code Name
46566 Neurophysiologic monitoring system

Identifiers

Type ID
Primary 00873263006795

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183123 000

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
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