FDA UDI In Commercial Distribution 🇺🇸 United States

GlidePath

DI: 00801741176517 · Model: 5587000R · Bard Peripheral Vascular, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GlidePath
Primary DI
00801741176517
Version / Model
5587000R
Catalog Number
5587000R
Company Name
Bard Peripheral Vascular, Inc.
Labeler DUNS
135057938
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-16
Public Version
1
Public Version Date
2021-08-24
Public Version Status
New
Public Device Record Key
ef5704ea-cad0-4730-99ea-7705e6e1e8fb

Device Description

GlidePath Retro Long-Term Hemodialysis Catheter Repair Kit

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
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
MSD Catheter, hemodialysis, implanted

GMDN Terms

Code Name
37278 Double-lumen haemodialysis catheter, implantable

Identifiers

Type ID
Package 10801741176514
Primary 00801741176517

Customer Contacts