FDA UDI In Commercial Distribution 🇺🇸 United States

iDrive Ultra

DI: 10884521510579 · Model: IDRVULTRA2 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iDrive Ultra
Primary DI
10884521510579
Version / Model
IDRVULTRA2
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-08
Public Version
8
Public Version Date
2023-04-24
Public Version Status
Update
Public Device Record Key
027d3b35-6078-4d51-b102-ef9431907683

Device Description

Reusable Powered Handle

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
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Dry Heat Sterilization

Product Codes

Code Name
GDW STAPLE, IMPLANTABLE

GMDN Terms

Code Name
62383 Motorized cutting stapler handpiece

Identifiers

Type ID
Primary 10884521510579

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K121510 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 120 Degrees Fahrenheit