FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 30845854034075 · Model: C8006 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
NA
Primary DI
30845854034075
Version / Model
C8006
Catalog Number
C8006
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2023-12-06
Public Version Status
Update
Public Device Record Key
3624dc82-15ef-42e6-a67a-d31564316cbe
Distribution End Date
2023-12-05

Device Description

NITINOL GUIDEWIRE, 0.8MM (.032 IN) X 356MM (14 IN), QTY 5

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
No
Has Lot/Batch Number
Yes
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
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Direct Marking 20845854034078
Primary 30845854034075
Unit of Use 00845854034074

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.8 Millimeter