FDA UDI In Commercial Distribution 🇺🇸 United States

PowerGlide Pro

DI: 00801741215889 · Model: PCK00007 · Bard Access Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PowerGlide Pro
Primary DI
00801741215889
Version / Model
PCK00007
Catalog Number
PCK00007
Company Name
Bard Access Systems, Inc.
Labeler DUNS
044611812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-13
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
228c552b-a024-4941-8c9f-d4898f560d94

Device Description

Catheter Placement Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
FOZ Catheter, intravascular, therapeutic, short-term less than 30 days

GMDN Terms

Code Name
32151 Peripheral vascular intervention infusion catheter

Identifiers

Type ID
Package 10801741215886
Primary 00801741215889

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8 Centimeter
Device Size Text, specify Gauge

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius