FDA UDI In Commercial Distribution 🇺🇸 United States

Transonic

DI: 00877466002240 · Model: HQE4FMV · TRANSONIC SYSTEMS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Transonic
Primary DI
00877466002240
Version / Model
HQE4FMV
Company Name
TRANSONIC SYSTEMS INC.
Labeler DUNS
101317451
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-08
Public Version
1
Public Version Date
2020-10-16
Public Version Status
New
Public Device Record Key
cbcedf8c-b6b8-4551-8054-8afad4d5b58e

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Ethylene Oxide", "Hydrogen Peroxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
DPW Flowmeter, Blood, Cardiovascular

GMDN Terms

Code Name
61227 Invasive vascular ultrasound system

Identifiers

Type ID
Primary 00877466002240

Premarket Submissions

Submission Number Supplement Number
K872048 000