FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00885074213019 · Model: DLP3W64R · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00885074213019
Version / Model
DLP3W64R
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-22
Public Version
4
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
e1f6d346-9f37-473d-83a8-4bc186934555

Device Description

CANNULA KIT DLP3W64R 5PK DR MCGEE

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
Package 20885074213013
Primary 00885074213019

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K924529 000