FDA UDI In Commercial Distribution 🇺🇸 United States

Barrx

DI: 10884521546295 · Model: AR-1000 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Barrx
Primary DI
10884521546295
Version / Model
AR-1000
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-16
Public Version
6
Public Version Date
2023-03-14
Public Version Status
Update
Public Device Record Key
b542319b-429b-42b3-bcb7-9dbf1e27fa8d

Device Description

Anorectal RFA Wand 15mm x 10mm

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
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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
61872 Endoscopic electrosurgical electrode, bipolar, single-use

Identifiers

Type ID
Primary 10884521546295

Customer Contacts

Device Sizes

Type Value Unit Text
Length 15 Millimeter
Width 10 Millimeter