FDA UDI In Commercial Distribution 🇺🇸 United States

Portex

DI: 15019315061073 · Model: 100/905/301 · Smiths Medical International Ltd
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Portex
Primary DI
15019315061073
Version / Model
100/905/301
Company Name
Smiths Medical International Ltd
Labeler DUNS
215590304
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-12
Public Version
3
Public Version Date
2022-10-24
Public Version Status
Update
Public Device Record Key
3ffc155d-aa82-4933-b709-07f0a17afd19

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
MR Conditional
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
No
Sterilization Prior Use
No

Product Codes

Code Name
BYE Attachment, breathing, positive end expiratory pressure
BTL Ventilator, emergency, powered (resuscitator)

GMDN Terms

Code Name
37706 Ventilator breathing circuit, single-use

Identifiers

Type ID
Package 35019315061077
Primary 15019315061073

Premarket Submissions

Submission Number Supplement Number
K123957 000