FDA UDI In Commercial Distribution 🇺🇸 United States

Emprint

DI: 10884521190764 · Model: CA190RC1 · Covidien LP
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Emprint
Primary DI
10884521190764
Version / Model
CA190RC1
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-01
Public Version
8
Public Version Date
2023-03-10
Public Version Status
Update
Public Device Record Key
45cb6d77-ee42-4455-9996-e7d6e07e8e23

Device Description

Ablation Reusable Cable

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
NEY SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES

GMDN Terms

Code Name
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Primary 10884521190764

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-22 – 158 Degrees Fahrenheit