FDA UDI In Commercial Distribution 🇺🇸 United States

Portex

DI: 10351688430922 · Model: H1041 · Smiths Medical International Ltd
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Portex
Primary DI
10351688430922
Version / Model
H1041
Company Name
Smiths Medical International Ltd
Labeler DUNS
215591523
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-29
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
8dc83247-18d4-4aa0-b1a3-46f439bfae5c

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
No
Sterilization Prior Use
No

Product Codes

Code Name
NHK RESUSCITATOR,MANUAL,NON SELF-INFLATING

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Package 30351688430926
Primary 10351688430922

Premarket Submissions

Submission Number Supplement Number
K970785 000