FDA UDI In Commercial Distribution 🇺🇸 United States

Compass International

DI: B169KCP200 · Model: KCP-20 · Compass International
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Compass International
Primary DI
B169KCP200
Version / Model
KCP-20
Catalog Number
KCP-20
Company Name
Compass International
Labeler DUNS
809466410
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-26
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
87b53e71-f4dd-42ed-beea-c31c171de1f7

Device Description

Kelly Coagulation Probe

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
HAW Neurological Stereotaxic Instrument

GMDN Terms

Code Name
61870 Open-surgery electrosurgical handpiece/electrode, monopolar, reusable

Identifiers

Type ID
Primary B169KCP200