FDA UDI Not in Commercial Distribution 🇺🇸 United States

PadPro

DI: 10653405042679 · Model: 2001P · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PadPro
Primary DI
10653405042679
Version / Model
2001P
Catalog Number
2001P
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
b258d9b7-8ca6-4766-aec1-29e0e46705ae
Distribution End Date
2023-09-06

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MKJ Automated External Defibrillators (Non-Wearable)

GMDN Terms

Code Name
45806 Multifunction cardiac electrode, adult

Identifiers

Type ID
Package 20653405042676
Primary 10653405042679

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K014209 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-20 – 55 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
0 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
5 – 35 Degrees Celsius