FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED

DI: 10845854030646 · Model: C5012A · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
CONMED
Primary DI
10845854030646
Version / Model
C5012A
Catalog Number
C5012A
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2023-12-05
Public Version
1
Public Version Date
2023-12-13
Public Version Status
New
Public Device Record Key
8842642d-43cc-47db-ba15-8a120b67f033

Device Description

ACROMIOPLASTY ELECTRODE (ELECTRODE ONLY)

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
No
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
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
61875 Endoscopic electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Unit of Use 00845854030649
Primary 10845854030646
Previous 20845854030643

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K823424 000