FDA UDI In Commercial Distribution 🇺🇸 United States

Portex

DI: 15019315056802 · Model: 100/126/050 · SMITHS MEDICAL MD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Portex
Primary DI
15019315056802
Version / Model
100/126/050
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
2020-12-01
Public Version Status
Update
Public Device Record Key
8ae5a6fd-00af-4854-b29f-b530958e8259

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BTR Tube, tracheal (w/wo connector)

GMDN Terms

Code Name
46967 Basic endotracheal tube, single-use

Identifiers

Type ID
Package 35019315056806
Primary 15019315056802
Package 55019315056800

Premarket Submissions

Submission Number Supplement Number
K790312 000