FDA UDI In Commercial Distribution 🇺🇸 United States

VENI-GARD

DI: 10653405014423 · Model: 730-4432 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
500

Basic Information

Brand Name
VENI-GARD
Primary DI
10653405014423
Version / Model
730-4432
Catalog Number
730-4432
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
500
Record Status
Published
Publish Date
2020-04-28
Public Version
2
Public Version Date
2023-09-04
Public Version Status
Update
Public Device Record Key
0e3c4394-bc7c-437c-8dcb-558f1fdf0b61

Device Description

Veni-Gard TM Jr.

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
KMK DEVICE, INTRAVASCULAR CATHETER SECUREMENT

GMDN Terms

Code Name
34864 Adhesive bandage

Identifiers

Type ID
Package 20653405014420
Primary 10653405014423
Unit of Use 00653405014426

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 32 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit