FDA UDI In Commercial Distribution 🇺🇸 United States

C-REAMER

DI: 10845854019177 · Model: 8787 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
4

Basic Information

Brand Name
C-REAMER
Primary DI
10845854019177
Version / Model
8787
Catalog Number
8787
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2022-12-22
Public Version
3
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
07fc6101-76fd-447c-a77c-169c46118296

Device Description

C-Reamer, Cannulated 7.0mm

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GFG BIT, SURGICAL

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Package 20845854019174
Primary 10845854019177
Unit of Use 00845854019170

Customer Contacts