FDA UDI In Commercial Distribution 🇺🇸 United States

Prodigy™ Catheter

DI: 00850032079075 · Model: PRODIGY8F-S · IMPERATIVE CARE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prodigy™ Catheter
Primary DI
00850032079075
Version / Model
PRODIGY8F-S
Catalog Number
PRODIGY8F-S
Company Name
IMPERATIVE CARE, INC.
Labeler DUNS
080816678
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-10
Public Version
5
Public Version Date
2023-12-15
Public Version Status
Update
Public Device Record Key
dc12ae02-2ee0-48eb-a6c6-993c03661019

Device Description

8F Short Prodigy™ 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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QEW Peripheral Mechanical Thrombectomy With Aspiration

GMDN Terms

Code Name
58173 Thrombectomy suction catheter

Identifiers

Type ID
Primary 00850032079075

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K214114 000

Device Sizes

Type Value Unit Text
Introducer Sheath Compatibility 8 French
Catheter Length 50 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place