FDA UDI Not in Commercial Distribution 🇺🇸 United States

CONMED

DI: 10653405050858 · Model: 000150 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

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Basic Information

Brand Name
CONMED
Primary DI
10653405050858
Version / Model
000150
Catalog Number
000150
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2025-10-21
Public Version Status
Update
Public Device Record Key
59fa82a0-2040-4276-a7b4-dfefd5d35e51
Distribution End Date
2025-10-20

Device Description

Reusable Marked Spring Tip Guidewire, 210 cm X 1.86 mm

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
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
KNQ Dilator, esophageal

GMDN Terms

Code Name
38834 Flexible endoscopic cytology brush, single-use

Identifiers

Type ID
Package 20653405050855
Primary 10653405050858
Unit of Use 00653405050851
Direct Marking 30653405050852

Customer Contacts

Device Sizes

Type Value Unit Text
Length 210 Centimeter
Outer Diameter 1.86 Millimeter