FDA UDI In Commercial Distribution 🇺🇸 United States

PowerPro

DI: 10845854028612 · Model: PRO6050 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PowerPro
Primary DI
10845854028612
Version / Model
PRO6050
Catalog Number
PRO6050
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2023-11-30
Public Version Status
Update
Public Device Record Key
f7b6dfaf-ef8f-4cce-9f44-9987f20c816f

Device Description

POWERPRO 1/8 IN KEYLESS CHUCK ATTACHMENT

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
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
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
Direct Marking 20845854028619
Primary 10845854028612

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.125 Inch