FDA UDI In Commercial Distribution 🇺🇸 United States

Portex

DI: 10351688410245 · Model: 002220 · Smiths Medical International Ltd
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Portex
Primary DI
10351688410245
Version / Model
002220
Company Name
Smiths Medical International Ltd
Labeler DUNS
215591523
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-28
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
2360f927-f2a5-42cc-9733-5c3e91e6edfd

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAF NEBULIZER (DIRECT PATIENT INTERFACE)

GMDN Terms

Code Name
35457 Benchtop nebulizer, non-heated

Identifiers

Type ID
Package 30351688410249
Primary 10351688410245

Premarket Submissions

Submission Number Supplement Number
K901315 000