FDA UDI In Commercial Distribution 🇺🇸 United States

Edge

DI: 10884521545571 · Model: SDK4900-FT · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Edge
Primary DI
10884521545571
Version / Model
SDK4900-FT
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2023-10-19
Public Version Status
Update
Public Device Record Key
fbd8ce3c-362e-4fad-8a38-4d7ba788cefd

Device Description

Firm Tip;Endobronchial Procedure Kit;90 Catheter

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JAK System, x-ray, tomography, computed

GMDN Terms

Code Name
57786 Bronchoscopic catheter

Identifiers

Type ID
Primary 10884521545571

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Second Outer Diameter,2.0,Millimeter;
Outer Diameter 2.68 Millimeter
Length 1069.5 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry