FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10653405064213 · Model: 1514848000 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
NA
Primary DI
10653405064213
Version / Model
1514848000
Catalog Number
1514848000
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2020-10-14
Public Version Status
Update
Public Device Record Key
82a6379a-2614-41f8-be76-5340256b0f5b
Distribution End Date
2020-10-13

Device Description

LEAD WIRE BULK PACK

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
No
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
No

Product Codes

Code Name
BZQ Monitor, breathing frequency

GMDN Terms

Code Name
35562 Electrocardiographic lead set, reusable

Identifiers

Type ID
Package 20653405064210
Primary 10653405064213
Unit of Use 00653405064216

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K912415 000