FDA UDI Not in Commercial Distribution 🇺🇸 United States

POWERPRO

DI: 10845854044247 · Model: PRO5095RFB · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
POWERPRO
Primary DI
10845854044247
Version / Model
PRO5095RFB
Catalog Number
PRO5095RFB
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-14
Public Version
10
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
d36cac8d-9058-4e8a-afa4-7bebfb2346bb
Distribution End Date
2022-06-09

Device Description

RFB, POWERPRO SYSTEM STERILIZATION CASE, SMALL

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
No
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
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Direct Marking 20845854044244
Primary 10845854044247

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090560 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY