FDA UDI In Commercial Distribution 🇺🇸 United States

WISONIC

DI: 06971355420765 · Model: P7-3T-H · SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
WISONIC
Primary DI
06971355420765
Version / Model
P7-3T-H
Company Name
SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD.
Labeler DUNS
543063066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-20
Public Version
1
Public Version Date
2021-08-30
Public Version Status
New
Public Device Record Key
91d9a973-292d-4430-b5bd-fc101753e2b4

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
MR Unsafe
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
ITX Transducer, Ultrasonic, Diagnostic

GMDN Terms

Code Name
37891 Oesophageal ultrasound imaging transducer, reusable

Identifiers

Type ID
Primary 06971355420765

Premarket Submissions

Submission Number Supplement Number
K210154 000