FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 20721902958797 · Model: DLP3E09R · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
NA
Primary DI
20721902958797
Version / Model
DLP3E09R
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-06-05
Public Version
5
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
2a6cef54-542a-44f3-8b2f-3665d6d68c3b
Distribution End Date
2018-10-24

Device Description

CANNULA KIT DLP3E09R 5PK AULTMAN

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Primary 20721902958797
Unit of Use 00721902958793

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K924529 000