FDA UDI In Commercial Distribution 🇺🇸 United States

POWERPRO

DI: 10845854028568 · Model: PRO3130 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
POWERPRO
Primary DI
10845854028568
Version / Model
PRO3130
Catalog Number
PRO3130
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-28
Public Version
2
Public Version Date
2022-06-30
Public Version Status
Update
Public Device Record Key
407b330d-4d50-4eaf-a9ef-4878d62e185f

Device Description

PowerPro Sterile Transfer Battery Shroud

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HAB SAW, POWERED, AND ACCESSORIES

GMDN Terms

Code Name
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Primary 10845854028568
Direct Marking 20845854028565

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K012320 000