FDA UDI In Commercial Distribution 🇺🇸 United States

DENALI® Vena Cava Filter

DI: 00801741040795 · Model: DL900J · Bard Peripheral Vascular, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DENALI® Vena Cava Filter
Primary DI
00801741040795
Version / Model
DL900J
Catalog Number
DL900J
Company Name
Bard Peripheral Vascular, Inc.
Labeler DUNS
135057938
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
16bc6725-638a-4cbf-ba2e-ab11003c202d

Device Description

DENALI® Vena Cava Filter Jugular/Subclavian

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
Yes
MRI Safety
MR Conditional
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
DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR

GMDN Terms

Code Name
44864 Vena cava filter, temporary/permanent

Identifiers

Type ID
Primary 00801741040795

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Working Sheath Length, 55 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Special Storage Condition, Specify
Special Conditions
Keep Away from Sunlight