FDA UDI In Commercial Distribution 🇺🇸 United States

VYGON

DI: 03660812040617 · Model: 9888.002 · VYGON
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VYGON
Primary DI
03660812040617
Version / Model
9888.002
Catalog Number
009888002
Company Name
VYGON
Labeler DUNS
392994778
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-21
Public Version
1
Public Version Date
2021-06-29
Public Version Status
New
Public Device Record Key
9cd92235-1ea7-4ccb-b711-8160b3525094

Device Description

Dualstopwhite male-female

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
No

Product Codes

Code Name
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

GMDN Terms

Code Name
31667 Catheter orifice occluder

Identifiers

Type ID
Package 33660812040618
Primary 03660812040617
Package 53660812040612

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius