FDA UDI In Commercial Distribution 🇺🇸 United States

Deltec

DI: 00610586024019 · Model: 21-2007-24 · SMITHS MEDICAL MD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Deltec
Primary DI
00610586024019
Version / Model
21-2007-24
Company Name
SMITHS MEDICAL MD, INC.
Labeler DUNS
106712748
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
5
Public Version Date
2021-01-08
Public Version Status
Update
Public Device Record Key
8117daf0-2276-49eb-91ac-b71c358dea14

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
LJT PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

GMDN Terms

Code Name
17180 Subcutaneous infusion/injection port needle

Identifiers

Type ID
Package 30610586024010
Primary 00610586024019

Premarket Submissions

Submission Number Supplement Number
K830730 000