FDA UDI In Commercial Distribution 🇺🇸 United States

Barrx

DI: 10884521516311 · Model: GW-005M · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Barrx
Primary DI
10884521516311
Version / Model
GW-005M
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2022-01-26
Public Version Status
Update
Public Device Record Key
88697654-c629-41d0-84b6-fa3bcdce66a5

Device Description

RFA Endoscopic Guidewire

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
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
No
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
46691 Gastro-urological guidewire, single-use

Identifiers

Type ID
Primary 10884521516311

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K935198 000

Device Sizes

Type Value Unit Text
Length 230 Centimeter
Outer Diameter 0.038 Inch