FDA UDI In Commercial Distribution 🇺🇸 United States

GlidePath

DI: 00801741187407 · Model: 5343230 · Bard Peripheral Vascular, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GlidePath
Primary DI
00801741187407
Version / Model
5343230
Catalog Number
5343230
Company Name
Bard Peripheral Vascular, Inc.
Labeler DUNS
135057938
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-08
Public Version
1
Public Version Date
2021-07-16
Public Version Status
New
Public Device Record Key
7d385895-a463-4ac9-8a33-de38bf30d93d

Device Description

GlidePath 13F Long-Term Hemodialysis Catheter Standard Kit, 23 cm

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 Safe
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 10801741187404
Primary 00801741187407

Customer Contacts

Device Sizes

Type Value Unit Text
Length 23 Centimeter
Catheter Gauge 13 French