FDA UDI In Commercial Distribution 🇺🇸 United States

PowerGlide

DI: 00801741142802 · Model: F118101DT · Bard Access Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PowerGlide
Primary DI
00801741142802
Version / Model
F118101DT
Catalog Number
F118101DT
Company Name
Bard Access Systems, Inc.
Labeler DUNS
044611812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-21
Public Version
3
Public Version Date
2024-01-08
Public Version Status
Update
Public Device Record Key
1faa81bc-5471-4511-a0e3-1241d9fc41d5

Device Description

PowerGlide Pro with Reinforced Tip, 18G 10cm, Max Barrier 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 10801741142809
Primary 00801741142802

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Gauge
Length 10 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius