FDA UDI In Commercial Distribution 🇺🇸 United States

Portex

DI: 55019315045514 · Model: 100/856/100 · ICU MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Portex
Primary DI
55019315045514
Version / Model
100/856/100
Company Name
ICU MEDICAL, INC.
Labeler DUNS
118380146
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
5
Public Version Date
2025-06-09
Public Version Status
Update
Public Device Record Key
65c14322-a057-46e9-9831-c352018f5224

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
BTO Tube, tracheostomy (w/wo connector)

GMDN Terms

Code Name
14089 Tracheostomy tube cannula, single-use

Identifiers

Type ID
Package 15019315045516
Package 35019315045510
Primary 55019315045514