FDA UDI In Commercial Distribution 🇺🇸 United States

Silicone PEG Guidewire System

DI: 00801741081231 · Model: 010063 · Bard Access Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Silicone PEG Guidewire System
Primary DI
00801741081231
Version / Model
010063
Catalog Number
010063
Company Name
Bard Access Systems, Inc.
Labeler DUNS
044611812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2021-04-12
Public Version Status
Update
Public Device Record Key
290bd0a4-a5d5-413c-aa36-734e763b1ffb

Device Description

Silicone PEG Guidewire System

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
No
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
KNT TUBES, GASTROINTESTINAL (AND ACCESSORIES)

GMDN Terms

Code Name
35419 Gastrostomy tube

Identifiers

Type ID
Package 20801741081235
Package 10801741081238
Primary 00801741081231

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 20 French