FDA UDI In Commercial Distribution 🇺🇸 United States

DLP®

DI: 20613994698333 · Model: 10053 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
DLP®
Primary DI
20613994698333
Version / Model
10053
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-05-21
Public Version
4
Public Version Date
2023-10-09
Public Version Status
Update
Public Device Record Key
4532375d-b58e-4794-a3f1-95ccb8cce589

Device Description

SUCTION 10053 6F SHAFT 10FR SOFT TIP 17L

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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
DTS SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS

GMDN Terms

Code Name
34923 Suction system catheter, general-purpose

Identifiers

Type ID
Primary 20613994698333
Unit of Use 00613994698339

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 6 FR Shaft
Device Size Text, specify 10 FR Soft Tip