FDA UDI In Commercial Distribution 🇺🇸 United States

PowerGlide Pro

DI: 00801741152849 · Model: F218101TX · Bard Access Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PowerGlide Pro
Primary DI
00801741152849
Version / Model
F218101TX
Catalog Number
F218101TX
Company Name
Bard Access Systems, Inc.
Labeler DUNS
044611812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-30
Public Version
2
Public Version Date
2024-01-09
Public Version Status
Update
Public Device Record Key
6b9d67bd-c355-4709-9b56-c6febfe1232d

Device Description

PG Pro 18G 10cm RT Full W/NG

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
Yes
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 10801741152846
Primary 00801741152849

Customer Contacts

Device Sizes

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

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius