FDA UDI In Commercial Distribution 🇺🇸 United States

TULSA-PRO

DI: 07540281000137 · Model: 106604 · Profound Medical Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TULSA-PRO
Primary DI
07540281000137
Version / Model
106604
Company Name
Profound Medical Inc
Labeler DUNS
243898678
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-25
Public Version
1
Public Version Date
2020-10-05
Public Version Status
New
Public Device Record Key
3ca3fa13-5a8d-4449-9106-a28290a4de9f

Device Description

TULSA-PRO Filter Box

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
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 07540281000137

Premarket Submissions

Submission Number Supplement Number
K202286 000