FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10845854029992 · Model: 8213 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10845854029992
Version / Model
8213
Catalog Number
8213
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
beece291-eea0-4867-809d-2f974ab1ae0e

Device Description

OSTEOTOME WITH MARKINGS

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
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Direct Marking 20845854029999
Primary 10845854029992

Customer Contacts