FDA UDI In Commercial Distribution 🇺🇸 United States

TULSA-PRO

DI: 07540281000151 · Model: 104008 · Profound Medical Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TULSA-PRO
Primary DI
07540281000151
Version / Model
104008
Company Name
Profound Medical Inc
Labeler DUNS
243898678
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-21
Public Version
4
Public Version Date
2020-08-19
Public Version Status
Update
Public Device Record Key
a4247e27-a4ba-4c20-8abc-dd7e8a1daa71

Device Description

TULSA-PRO Ultrasound Applicator

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
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
PLP High Intensity Ultrasound System For Prostate Tissue Ablation

GMDN Terms

Code Name
57888 Therapeutic oncological/gynaecological ultrasound system

Identifiers

Type ID
Primary 07540281000151

Premarket Submissions

Submission Number Supplement Number
K191200 000