FDA UDI In Commercial Distribution 🇺🇸 United States

Foot Control 3502 / 6302

DI: 10841736112226 · Model: 18-443-10 · SKYTRON LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Foot Control 3502 / 6302
Primary DI
10841736112226
Version / Model
18-443-10
Company Name
SKYTRON LLC
Labeler DUNS
078375583
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-15
Public Version
1
Public Version Date
2019-10-23
Public Version Status
New
Public Device Record Key
6a9d2728-19f3-4395-a979-8f3d52679e3f

Device Description

Foot Control 3502 / 6302

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FQO Table, Operating-Room, Ac-Powered

GMDN Terms

Code Name
36336 Foot-switch, electrical

Identifiers

Type ID
Primary 10841736112226

Customer Contacts

Phone
800-759-8766

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius