FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED

DI: 10845854037812 · Model: 25.1007 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
CONMED
Primary DI
10845854037812
Version / Model
25.1007
Catalog Number
25.1007
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-27
Public Version
1
Public Version Date
2023-12-05
Public Version Status
New
Public Device Record Key
7e30aa76-05fc-459c-bbd6-1bbe6ce22f0e

Device Description

4MM STRAIGHT RASP, OSTEOPREP

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
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
HRX Arthroscope

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Direct Marking 20845854037819
Primary 10845854037812
Previous 30845854037816

Customer Contacts