FDA UDI In Commercial Distribution 🇺🇸 United States

Niagara catheter

DI: 00801741075070 · Model: 5591000 · Bard Access Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Niagara catheter
Primary DI
00801741075070
Version / Model
5591000
Catalog Number
5591000
Company Name
Bard Access Systems, Inc.
Labeler DUNS
044611812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-04
Public Version
3
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
af2d6ec9-8948-4c88-be24-fd5706cd2854

Device Description

Niagara Catheterless Tray

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
MPB CATHETER, HEMODIALYSIS, NON-IMPLANTED

GMDN Terms

Code Name
37278 Double-lumen haemodialysis catheter, implantable

Identifiers

Type ID
Package 10801741075077
Primary 00801741075070

Customer Contacts