FDA UDI Not in Commercial Distribution 🇺🇸 United States

Arthroloop

DI: 20884521180649 · Model: 160300 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthroloop
Primary DI
20884521180649
Version / Model
160300
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2024-01-17
Public Version Status
Update
Public Device Record Key
3069181e-581b-4314-92b7-b54106d8c38c
Distribution End Date
2018-02-14

Device Description

Suture Passing Device

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
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
57874 Suturing unit, single-use

Identifiers

Type ID
Package 10884521180642
Primary 20884521180649

Customer Contacts