FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED FLEXITIP

DI: 30653405051187 · Model: 000218 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
CONMED FLEXITIP
Primary DI
30653405051187
Version / Model
000218
Catalog Number
000218
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2021-10-05
Public Version
1
Public Version Date
2021-10-13
Public Version Status
New
Public Device Record Key
9f05def2-c390-434b-9efc-7506f9e9aca8

Device Description

CONMED FLEXITIP DISPOSABLE SCLEROTHERAPY NEEDLE

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
Yes
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
GAA NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

GMDN Terms

Code Name
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Package 10653405051183
Primary 30653405051187
Unit of Use 00653405051186

Customer Contacts

Device Sizes

Type Value Unit Text
Weight 25 Gram
Length 5 Millimeter
Length 230 Centimeter
Outer Diameter 2.3 Millimeter