FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 20845854026073 · Model: 9735BA · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
20845854026073
Version / Model
9735BA
Catalog Number
9735BA
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2023-12-06
Public Version Status
Update
Public Device Record Key
4d66727e-5265-4dfc-b49e-281c7aba8680
Distribution End Date
2023-12-05

Device Description

MENISCECTOMY ELECTRODE BASIC KIT; STANDARD DESIGN

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
Yes
Sterilization Methods
["Radiation Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
44093 Arthroscopic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 20845854026073

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K823424 000