FDA UDI In Commercial Distribution 🇺🇸 United States

VYGON

DI: 03660812075787 · Model: 896.038 E · VYGON
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VYGON
Primary DI
03660812075787
Version / Model
896.038 E
Catalog Number
896.038 E
Company Name
VYGON
Labeler DUNS
392994778
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
5
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
0a5792d2-cb8e-4852-beb4-9405db6c01bc

Device Description

Bionector

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
Yes
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
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days

GMDN Terms

Code Name
42750 Neutral-pressure intravenous line needleless valve-connector

Identifiers

Type ID
Package 33660812075788
Primary 03660812075787
Package 53660812075782

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius