FDA UDI In Commercial Distribution 🇺🇸 United States

Footswitch

DI: 00817183020011 · Model: 9-001-00 · NORTHGATE TECHNOLOGIES INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Footswitch
Primary DI
00817183020011
Version / Model
9-001-00
Catalog Number
9-001-00
Company Name
NORTHGATE TECHNOLOGIES INC.
Labeler DUNS
627969264
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-26
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
f6ff4ff9-490c-4491-b702-bd78da99c8da

Device Description

Pneumatic footswitch for use with Lithotripters

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FFK Lithotriptor, Electro-Hydraulic

GMDN Terms

Code Name
35711 Electrohydraulic lithotripsy system

Identifiers

Type ID
Primary 00817183020011

Premarket Submissions

Submission Number Supplement Number
K923822 000