FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10845854028650 · Model: PRO6232-4 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10845854028650
Version / Model
PRO6232-4
Catalog Number
PRO6232-4
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-14
Public Version
2
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
30642454-1320-4dc5-8833-1a72cbb7a3b7

Device Description

2-Trigger 4mm Pin Driver

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
No

Product Codes

Code Name
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
44106 Patient health record information system application software

Identifiers

Type ID
Primary 10845854028650
Direct Marking 20845854028657

Customer Contacts