FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall SCD

DI: 10884521082601 · Model: 95255 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kendall SCD
Primary DI
10884521082601
Version / Model
95255
Catalog Number
95255
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-21
Public Version
8
Public Version Date
2019-11-04
Public Version Status
Update
Public Device Record Key
7800a0ae-e3ee-4876-a409-307fc51355bd

Device Description

Express Sequential Compression System Vascular Refill Detection

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
No
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
JOW SLEEVE, LIMB, COMPRESSIBLE

GMDN Terms

Code Name
44785 Sequential venous compression system pump

Identifiers

Type ID
Primary 10884521082601

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
15 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-4 – 131 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Keep dry;AVOID DIRECT SUNLIGHT