FDA UDI In Commercial Distribution 🇺🇸 United States

DOPPLEX

DI: 05051968031747 · Model: DR4-USA · HUNTLEIGH HEALTHCARE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DOPPLEX
Primary DI
05051968031747
Version / Model
DR4-USA
Catalog Number
DR4-USA
Company Name
HUNTLEIGH HEALTHCARE LIMITED
Labeler DUNS
217207083
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-25
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
ecca4b94-ee83-445c-8d96-ee77b615d571

Device Description

DOPPLEX REPORTER DR4 USA

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KNG Monitor, Ultrasonic, Fetal

GMDN Terms

Code Name
44106 Patient health record information system application software

Identifiers

Type ID
Primary 05051968031747

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K930200 000